Specialisms
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Data
We connect programmers, statisticians, data managers and data scientists with the latest opportunities across a variety of life science industries.
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Clinical
In support of some of the most innovative pharmaceutical and biotechnology companies and leading CROs, our team source professionals for stages I - IV clinical trials across Europe and the US.
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Technical Operations
From manufacturing to product development, facilities management to engineering, our team understand the skills necessary to ensure the success of a tech ops department.
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Commercial
From sales and business development through to account management, our commercial team find talent across all post-trial drug development stages.
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Technology
Many of our most longstanding partners operate in the technology sectors, from ERP/CRM to machine learning and artificial intelligence.

Find your next role.
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[E] (Sr) Data Team Lead
England |
Negotiable
Are you ready to embark on a meaningful career that will have a positive impact on millions of people worldwide?As one the worlds leading CROs, they pride themselves on have a highly supportive culture with an impressive track record of internal career progression through mentoring and developing their people.They are now looking to bring onboard a Senior Data Team Lead.As the Senior Data team lea you will lead a team of DTL's and serve as the primary contact on Data Management deliverables and manage a program of studies, some which are on a Global scale.Teamwork is everything, and you will have the opportunity to build relationships across the wider Data Operations team, including functional leads, project managers and senior stakeholders to ensure shared milestones and quality deliverables are met.To be successful in this role you will need:Knowledge of Good Clinical Practices (GCP) and relevant regulatory guidelines.Great communication, interpersonal, customer service, and teamwork skills.Excellent organizational and problem-solving skills.Proven project management skills.Track record of personal development and developing others.Independently managing SOW's & budgets.Ability to lead and support a team.
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Quality Manager
Weil am Rhein |
£85000 - £90000 per annum
Job Title: Quality ManagerMy client, one of the largest pharmaceutical company in the world, is looking for a GMP Quality Manager to work in their facility located on the German/Swiss border and be responsible for the quality direction of the facility and maintaining the Quality Management System.Salary and benefits: 85,000EUR - 90,000EUR (Depending on experience)Flexibility on remote working.Role and Responsibilities: You will be named Quality person on licensing, as appropriate.Responsibility for the maintenance of the Quality Management System.Organise and distribute work to the Quality team staff.Reviewal and writing quality documents.Management of the SOPs including EDMS, Archiving and change control.Perform internal audits to determine compliance to the quality system and identifying areas of improvement.To ensure during review documentation is correct, GMP compliant, error-free and entered in the operating systems appropriately.Identify and support investigations for any identified internal and/or external non-conformances.Support risk management, including evaluating risk assessments.Develop and provide Quality Assurance/Quality Control training for the Quality department.Required skills and qualifications:You must speak, read and write in English.Experience and strong knowledge of GMP regulated environmentsExperience with, and implementation of cGMP's, GLP, GCP, calibration and validation.Valid driver's license and good driving record (Traveling to client sites as needed and assigned).Knowledge of local GMO regulations.Bachelors or Masters degree in a science related field.If you want to have the opportunity to work for one of the biggest pharmaceutical and have a positive impact on millions of people worldwide all while earning an attractive salary. Then apply for this position below to put yourself under immediate consideration by sending your CV to jonathan.smith@seclifesciences.com or call +49 69 22222888. Interviews are expected to take place at the end of this month. Please note, this company requires the candidate to own an EU work permit.
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CDISC Expert / Statistical SAS Programmer - Big Pharma UK
England |
High Benefits, Relocation Package
Company: Mid-Size PharmaRemote based position in the UK + 1 day/week onsite, London area.Very competitive packageAs a CDISC Technical Expert / Principal or Senior Manager level, you will be expected to cover the following responsibilities:- Taking leadership of the statistical programming activities- Creating analysis datasets, tables, listing and figures from clinical trial data- Develop and validate analysis and reporting deliverables on the safety and efficacy side of programming- Collaborate effectively with an international team of programmers. Required Skills and Qualifications: - BSc in Computer Science, Applied Mathematics, Life Sciences or related fields; - Minimum 6 years of statistical programming in clinical trials + Leading Project.- Extended CDISC, SAS Programming skills, including MACRO, Graphs, and TFLs - tables, figures and listings- Solid knowledge of the drug development cycle and related guidelines- Strong analytical mid-set with a particular focus on details- CDISC experience would be a massive advantage - Excellent communication skills in English, both verbal and writtenDo not hesitate to apply or contact me for more details about this role to: Yanick Millet Associate Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 yanick.millet@seclifesciences.com
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Senior Biostatistician, Biotech Pharma
France |
Negotiable
A well-established biotech company in the clinical research environment is currently hiring a Senior Biostatistician (Early phase I - II and phase III + submission in the future) to join the Biometrics team. The position is remote based in France + onsite visit on monthly basis (1h from Paris).You will be part of a large organisation with strategic partnership in the pharmaceutical industry allowing you to grow and develop a long term career in the business.As an experienced Biostatistician you will be expected to cover the following responsibilities: - Performing advanced scientific statistical analyses- Statistical part of the protocol development and statistical support for clinical studies (i.e.: statistical review, sample size, statistical analysis…) - Writing of the statistical analysis plan - Representing Biostatistics as a member of clinical trial teams, providing input and technical guidance to elicit meaningful and/or productive outcomes. - Presentation of statistical results- Collaborating with statistical programming and other functions to ensure timely delivery of TFLs with good quality.- Implementing design and analysis methods at the study level and participates in Statistical Review Forum (SRF) discussions of studies assigned to others.Requirements:- MSc or PhD statistics, biostatistics, or related field - Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment - Experience developed across Phase I to III studies - Good experience with SAS and R statistical software - Fluent in English (spoken and written) - Ability to work in team and independently - Demonstrated understanding of advanced statistical methods used in drug development- Ability to show critical thinking with logical problem-solving- Excellent written and verbal communication skills- Excels in a team environmentPlease contact me at yanick.millet@seclifesciences.com for more information.
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Process & Clinical Data Manager - Pharma
France |
Negotiable
Position : Senior Clinical Data Manager, Clinical and Process DevelopmentDepartment : BiometricsCompany : Biotech company, OncologyLocation : France, remote + officeWorking condition : Remote based position in France with business travel onsiteMy partner is an exciting Biotech at clinical stage, with a auspicious pipeline in Oncology. To support the Biometrics department, we are recruiting a Senior Clinical Data Manager with a strong background in CRO oversight from the sponsor's side, CDISC - SDTM experience and able to enhance the existing process.The Senior CDM will be :- the main contact for data management subcontractors;- in charge of defining and implementing the processes needed to ensure that the clinical data are consistent and reliable;- coordinate all the stakeholders involved in the data flow from different sources.The Senior CDM will work closely with Clinical Research Directors, Clinical Trial Managers, Safety Manager, in addition to Biostatisticians and other Data Manager as well as a tight interactions with other functions including program management, bioinformatics, clinical pharmacology, and translational research.Responsibilities :- Contributing to the evaluation and selection of the CROs (Contract Research Organizations) for data management questions- Overseeing the data management subcontractors concerning the eCRF/EDC design, setup, testing- Supervising, reviewing, and validating the data management documents (e.g. data management plan and data validation plan, ...)- Planning and implementing data quality review, including programming of checks, conducting review meetings, following up on resolution of findings, ...- Ensuring that CROs comply with procedures and regulatory requirements- Management of internal/external data flow- Defining and implementing the data flow process from different vendors and internal research labs toward the clinical database- Reviewing and validating the data transfer specifications (DTS)- Checking the compliance of external data with respect to the DTS; Managing the resolution of data inconsistencies and reconciliation with clinical database- Defining and implementing the process of access and protection of the clinical data, in compliance with good clinical practices and regulatory requirements (GDPR)- Development of internal operating procedures - Developing standard operating procedures for the internal data management activities- Contributing to the development of standard as well as study specific eCRF forms- Developing and validating robust internal tools for capturing internal research dataRequirements:- Bachelors or master's degree in Data Management, Life Sciences, Informatics, Biostatistics or similar- At least 5-year experience in Data Management in a CRO or pharmaceutical R&D including oncology trials- Experience in CROs oversight- knowledge of CDISC/SDTM standardNice to Have:- Experience of interactions with FDA for BLA (Biologics Licence Application)- Experience in rare disease- Experience in a biotech company and/or small biometrics unit- Experience with eCRF/EDC systems- understanding of SAS, mainly for reporting- Knowledge of ICH, FDA, and GCP regulations and guidelinesCompetitive package + benefitsPlease contact me at yanick.millet@seclifesciences.com.
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(Senior) Clinical Data Manager - Lead projects
England |
£55000 - £65000 per annum + Annual bonus
One of my business partners is recruiting for a Data Manager to join the Biometrics team. The right profile will lead 3 to 5 projects supporting clinical trials from phase I to phase III (oversight, resources, timeline etc.) and will receive a solid mentoring support during the first 6 months.This position is 100% home based in Europe/UK and the company is focus on the well being and the innovation.The role could be FSP dedicated to 1 partner or multi-sponsors (depends on the candidate's preferences).Requirements:- At least 2 years experience in Clinical Data Management including project management responsibilities- Capable of providing quality control review for Data cleaning and identifying solutions and process improvements - Capable of training and mentoring others- Excellent communicationIf you are interested, please contact Yanick Millet, Principal Consultant Biometrics - SEC Life Sciences:Tel:+44 (0) 330 052 8373 / +33 (0) 1 70 80 74 89Email: yanick.millet@seclifesciences.com
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Senior / Principal Biostatistician - Europe (home-based)
France |
€60000 - €75000 per annum
Fantastic opportunity to join one of the leader in clinical trials, supporting Global Pharma and Biotech.This position could be 100% Home based from UK, France, Germany, Italy, Spain, Portugal, Romania, Poland etc.To be successful in this role you will have the following profile: - MSc or PhD statistics, biostatistics, or related field - Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment - Experience developed across Phase I to IV studies - Strong SAS skills - Fluent in English (spoken and written) - Ability to work in team and independently - Previous experience with home based work is ideal If you are interested, reach out to me at : yanick.millet@secpharma.com with your CV updated and your best availabilities to set up a call.Yanick Millet Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 Email: yanick.millet@seclifesciences.com www.linkedin.com/in/yanick-millet-b6273b30/
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Principal Statistician - Biopharma - Home Based in Europe
England |
Negotiable
Principal Statistician - Biopharma - Remote Based in EU We are recruiting for an exciting Principal Statistician with an innovative Biopharma to join them on permanent and remote basis anywhere across Europe. The company has an outstanding working culture where science is at the core of their activities, having products already approved and commercialized, they offer a unique blend of activities where a creative, technical individual can thrive, and impact meaningful products applied to oncology space. Key Responsibilities*Provide expertise into design, analysis and interpretation of clinical studies*Lead / oversee statistical and programming teams in relation to analyses *Provide statistical oversight and guide to study teams and CROs*Contribute and support to the statistical reports, briefing books, submissions, health authorities' request, and publications*Participate in interactions with health authorities*Contribute to internal process improvement and new statistical capabilities You will have:*MSc (or PhD) in mathematics, statistics with a strong statistical component.*Hands-on experience in designing and data analysis in clinical trials*Experience of modelling and simulation techniques to explore complex study designs*Strong programming skills in SAS or R*Ability to independently assess statistical programs and outputs for identification of correct/incorrect results*Excellent communication skills with great ability to adapt to a wider audience Nice to have Experience:*Oncology experience applied in clinical development *Bayesian design *Process improvement applied to statistical activities *Proficiency in French *Working experience in a multicultural environment*External vendors management If you looking to learn more about this exciting Principal Statistician role do not hesitate to get in touch for a confidential chat, alternatively send your CV to:Catalin ZahariaLead Consultant - Biometrics SAS Programming, Biostatistics, Data Management Tel: +44 (0) 207 255 66 65Catalin.Zaharia@seclifesciences.comlinkedin.com/in/catalindoruzaharia
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Senior / Principal Biostatistician - Europe (home-based)
Italy |
Negotiable
Fantastic opportunity to join one of the leader in clinical trials, supporting Global Pharma and Biotech.This position could be 100% Home based from UK/EUROPETo be successful in this role you will have the following profile: - MSc or PhD statistics, biostatistics, or related field - Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment - Experience developed across Phase I to IV studies - Strong SAS skills - Fluent in English (spoken and written) - Ability to work in team and independently - Previous experience with home based work is ideal If you are interested, reach out to me at : yanick.millet@secpharma.com with your CV updated and your best availability to set up a call.Yanick MilletPrincipal Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 - +33 (0) 1 70 80 74 89Email: yanick.millet@seclifesciences.comwww.linkedin.com/in/yanick-millet-b6273b30/
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Clinical Data Manager
Switzerland |
Negotiable
Do you want to embark on a new journey and build a career in a field where you can help millions of people around the world?My client, based in Geneva - Switzerland, is a well-established medical device company operating in the dermatology field with many high-end products in the market. They are a rapidly growing company who are looking to expand the team and you would be an integral part of that growth.You will collaborate with the rest of the team internally and with vendors externally on projects. You will be given a level of responsibility that will make you feel valued and appreciated.What's in it for you?*Great opportunity to grow professionally in an established company*You can decide how you want to take that growth*You will be an integral part of a growing team*Training and support are always offered and encouragedYour main responsibilities:*Responsible for all data management activities in compliance with guidelines and internal SOPs*Manage the query management process and database updates*Accountable for the review of clinical data for accuracy and consistency*Perform quality control and user acceptance testing*Develop and maintain all data management clinical study documents*Responsible for the filing and archiving of data management related documents*Work with external providers and coordinate the DM activities for outsourced clinical studies*Work closely and collaborate with other members of the teamWhat you will bring:*Minimum BSc degree in scientific or relevant field*3-5 years' experience as a Clinical Data Manager (at least 2 years in Pharma/CRO/Biotech)*Proven experience using EDC systems and reporting tools*Knowledge of ICH-GCP guidelines and medical terminology*Strong Excel skills*Experience with IBM is appreciated, but not required*Knowledge of biostatistics, SAS and SQL is a plus, but not required*Fluency in French and EnglishIf you are interested, apply to be immediately considered and to find out more information, feel free to reach out to me.
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Database Developer
Germany |
Negotiable
I'm currently exclusively working on an exciting new project for a German medical device client of mine who are looking for a Database Developer on long term freelance basis.Requirements:- Experience with BLOB Storage and SQL Databases - Hands on programming experience in Python- Recent expertise in cloud technologies and data transfers (Azure) - Fluent verbal and written English- EU citizen (This project can be operated remotely) - Experience with data storage in the life science sector is preferred
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Quality Engineer
Hampshire |
£30000 - £35000 per annum
Job Title: Quality EngineerThis is a great opportunity to work for one of the world's leading manufacturers and marketers in the cosmetics industry. Sold in over 150 countries, reaching over half a billion consumers each year. They are looking for a Quality Engineer to be responsible for the design and execution of Quality Engineering projects.Salary and benefits:£35,000 Salary.Role and Responsibilities: Monitor and guarantee compliance to GMP and adhere to defined processes.Supporting Plant and Global systems to safeguard conformity in GMP, Data Integrity and General Data Protection Regulation (GDPR) Implement new system and running practices to enhance procedure and product satisfactory while preserving compliance to regulatory requirements.Train employees in QA and Lean techniques, while coaching other employees of quality when carrying out work related to QE functions.Work in collaboration with suppliers, production, and developers in conversing standards and range boards. Share your expertise and proved support for investigations in complaints and CAPA's.You will be asked to document processes and procedures and technical reports.Analyse data/KPI's and propose suitable action. Carry out Audits and capability studies as needed.Assure a safe working environment through process adherence and hazard elimination/mitigation. Required skills and qualifications:Experience in either Pharmaceutical or Cosmetics industry.A solid understanding of Good Manufacturing Practices and adaptability when needed.Knowledge in quality management systems, process improvement, quality tools and process improvement utilising statistical problem-solving procedures. A desire and ability to coach other people.Familiarisation with Microsoft Office and SAP applications.An excellent opportunity to receive some amazing benefits while earning a competitive salary. This is your chance to take the next step in Quality Engineering and potentially further your career in Quality with their impressive career progression scheme.If you think you have what it takes and put yourself under immediate consideration, then apply below or send your CV to: jonathan.smith@seclifesciences.com or call +496922222888Interviews are expected to take place within the end of next month. You must be eligible to work in the UK for this position.
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Principal Biostatistician
Germany |
€80000 - €100000 per annum
Do you want to embark on a new journey and build a career in a field where you can help millions of people around the world?My client - based in south-west Germany - is a small sized biopharmaceutical company who work within the immuno-oncology field. They are building out the team in anticipation of their promising pipeline and are currently looking for a new Principal Biostatistician. The company's primary aim is to make innovative strides in the fight against cancer and provide patients with a new sense of hope. This is an amazing objective that you could be a part of!What's in it for you?*A chance to be a part of growing team and company*Great potential for growth within the company*A competitive wage and package*Flexible remote working offeredMain responsibilities:*Work closely and collaborate with the other members of the team*Participate in the writing of study protocols, clinical study report & statistical analysis plans*Perform analyses and generate outputs of clinical and biomarker data on study and program level (pooled data)*Oversee and be responsible for communications with CROs regarding statistical and programming deliverables*Communicate within a cross-functional team which include different scientific and operational disciplines*Some hands-on work, with tasks including interim analysisWhat you will bring:*Master/Diploma/PhD in statistics, maths, or a related discipline*Knowledge within the pharmaceutical industry - ideally at least 5 years' experience*Proven statistical programming skills. Preferably with R and/or SAS*Knowledge within oncology is not required, but a huge bonus*Ideally experience working in phase I, II and III trials*Experience with CDISC, Adam & STDM standards*Experience with extensive biomarker analyses*Excellent written and oral skills in in English*German is not required, but a bonusIf you are interested, apply to be immediately considered and to find out more information, feel free to reach out to me for a further discussion.
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Research Scientist - Protein Design/Machine Learning
Massachusetts |
US$98000 - US$148000 per annum + 401K, Healthcare, Life Insurance
Exciting Computational Biologist / Computational Modeler opportunityI'm working with a next-generation industrial biotechnology company who are seeking a computational biologist/modelerThis role will offer you:- Opportunity - Professional advancement for results-orientated team members- Accountability - Resources needed to succeed and the freedom to make it happen- - Passion - A work environment that challenges and promotes hard work that comes with working on the cutting edgeYou will be responsible for:- Developing predictive models for enzyme engineering using ML/DL techniques- Utilizing the data to enhance your ML/DL models- Using 3D structures to increase enzyme stabilityYou will have:- Ph.D. in Bioengineering, Biochemistry, Chemical Engineering, Computer Science, or a related field- Knowledge and experience in protein modelling or design using Rosetta- Knowledge of data science methods- Fluent in programming in a Linux environment using PythonIf interested, then send over your resume to Luca.marcovecchio@seclifesciences.com or alternatively, reach out for a confidential chat with me!
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Clinical QA Manager (12 months)
Frankfurt (Oder) |
Negotiable
Clinical quality manager(contract, 12 months)Frankfurt, GermanyHybridAs part of their on-going growth, a Global Pharmaceutical company are in search of a Clinical Quality manager at their site based just outside of Frankfurt. This job is your opportunity to join a global leader in pain management on their journey of moving towards a world free of pain. Using your expertise, you'll be responsible for setting up and maintaining a QA system whilst acting as subject matter for any GCP related topics.What's in it for you?· Competitive rates and excellent lifestyle balance· Working with innovative medicines aiming to meet the needs of patients living with rare diseases· Improving the lives of thousands· Rewarding work in a friendly and supportive work environmentYour main responsibilities:· Act as subject matter expert for GCP related topics (Cross-fucntional)· Conduct GCP audits (system audits, trial master file audits, site audits, vendor qualification)· Support quality-related authority inspections, also supporting vendor audits· Review of quality event documentation such as Deviation investigations, Change Controls and CAPAWhat you'll bring:· Completed scientific studies (biology, biotechnology, pharmacy or similar) or technical training (BTA, CTA or MTA) or comparable qualification· Several years of professional experience (at least 3 years) in the regulated environment of the biotechnological or pharmaceutical industry within GCP requirements· Strong knowledge and practical experience in the field of quality assurance/ quality management· Previous GCP auditing Experience within Pharmaceutical industryFor more information on this position reach out to brook.bridges@seclifesciences.com or apply now for immediate consideration
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Biostatistician (Senior & Principal) - Boutique CRO
Germany |
€55000 - €75000 per annum
An exciting opportunity is available for experienced Statisticians to join a growing Specialised CRO on remote basis across Europe. The company has contributed to the developed of key products in demanded therapeutic areas and their consultative and quality focused approach puts them apart from their competitors. As (Senior / Principal) Biostatistician you will:- Apply knowledge of statistics to independently provide statistical consulting - Provide support with study design and protocol development- Review project related documents- Write statistical programs to generate datasets, tables, listings, figures;- Collaborate close with cross-functional departments such as data management, medical writing, etc. - Support ISS and ISE for regulatory submissions;- Collaborate effectively with project team members;You will be successful if you have:- MSc in Statistics, Applied Mathematics, Life Sciences, or related field; - Minimum 3 years of leading clinical studies;- Experience in applying statistical methodologies common in clinical trials;- Excellent communication skills and ability to adapt to different audiences;- Knowledge in CDISC standards would be advantageous;If you are interested in learning more about this great opportunity, do not hesitate to get in touch with Catalin at catalin.zaharia@secpharma.com or feel free to call him at +44 (0)20 7255 6610#biostatistics #statistics #sas #r #clinicaldevelopment #ADaM #biotech #CRO #Pharma #clinicaltrials
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Associate Director, Biostatistics - Swiss Biopharma
Switzerland |
Swiss Franc170000 - Swiss Franc185000 per annum + Benefits
SEC has been appointed to recruit on behalf of their client, an innovative Biopharma, an Expert Statistician to join the growing biometrics team.As Associate Director, Statistics you will oversee statistical activities in oncology studies. You will contribute to writing appropriate protocol sections and or review analysis plans and define appropriate methods and procedures for statistical analysis. Furthermore you will ensure that proper validation for statistical tables and listings are being implemented. Additionally, you will generate and review statistical documents and reports required for regulatory submissions.This opportunity suits excellent someone who has a strong technical experience developed in clinical trials, with a deep passion towards statistics. The role is a technically focused and is not involving people management.The successful candidate will have:- MSc in Statistics or related fields;- Strong experience in statistical analysis in a clinically related subjects;- Experience in study oversight and coordinating a team;- You have good SAS or R programming skills;- Demonstrable knowledge of international standards (ICH, GCP, CDISC) and regulations related to clinical studies;- Solid communication skills and ability to adapt to non-technical audiences;- Ability to demonstrate teamwork;- Extensive statistical experience in Oncology area.This opportunity will suit an experienced individual looking to contribute to the bigger picture and support authorization of innovative products and help lives of million of patients out there. You will have a scientific driven activity where working close with clinical team in supporting regulatory submissions.Do not hesitate and get in touch for a confidential chat about this Expert Statistician role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - #BiometricsSAS Programming, #Biostatistics, Data Management Tel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Senior Clinical Data Manager - UK & Europe (remote)
England |
€50000 - €65000 per annum + Bonus & Benefits
An exciting opportunity is available for experienced Clinical Data Managers to join a well established CRO on remote basis. The company has developed superb expertise within key therapeutic indications and has secured strategic relationships with specialized Biotech and Medical Devices companies.This is an FSP role - you will have the scientific exposure associated with activities developed in a global Pharma, while benefit from the remote flexibility coming from the CRO employment. As Lead Data Manager you will be responsible of all Data Management activities on project level, essentially you will take leadership on study level and ensure quality deliverables on time and within budget. You will act as SME - subject matter expert - and provide leadership and vision to the team, drive process standardisation and manage vendors.The successful candidate will have:- BSc in life sciences with minimum 3 years of DM experience within pharma sector; - End-to-end experience (from setting-up to delivering clean database locks);- Excellent communication skills - able to manage clients and internal teams;- Ability to work in a multicultural environment;- Proactive, team-oriented attitude;- RAVE experience would be a strong advantage;If you're looking to work with a global organization that will provide excellent development opportunities, this is the right opportunity for you! You will work close with some of the brightest individuals in life-changing projects helping and transforming the millions of patients out there. Don't hesitate and get in touch for a confidential chat about this Lead Data Manager role and please send your updated CV to:Catalin ZahariaPrincipal Consultant - BiometricsData Management, Statistical Programming, Biostatistics Tel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Associate Director, Biostatistics - Swiss Biopharma
Switzerland |
Swiss Franc170000 - Swiss Franc185000 per annum + Benefits
SEC has been appointed to recruit on behalf of their client, an innovative Biopharma, an Expert Statistician to join the growing biometrics team.As Associate Director, Statistics you will oversee statistical activities in oncology studies. You will contribute to writing appropriate protocol sections and or review analysis plans and define appropriate methods and procedures for statistical analysis. Furthermore you will ensure that proper validation for statistical tables and listings are being implemented. Additionally, you will generate and review statistical documents and reports required for regulatory submissions.This opportunity suits excellent someone who has a strong technical experience developed in clinical trials, with a deep passion towards statistics. The role is a technically focused and is not involving people management.The successful candidate will have:- MSc in Statistics or related fields;- Strong experience in statistical analysis in a clinically related subjects;- Experience in study oversight and coordinating a team;- You have good SAS or R programming skills;- Demonstrable knowledge of international standards (ICH, GCP, CDISC) and regulations related to clinical studies;- Solid communication skills and ability to adapt to non-technical audiences;- Ability to demonstrate teamwork;- Extensive statistical experience in Oncology area.This opportunity will suit an experienced individual looking to contribute to the bigger picture and support authorization of innovative products and help lives of million of patients out there. You will have a scientific driven activity where working close with clinical team in supporting regulatory submissions.Do not hesitate and get in touch for a confidential chat about this Expert Statistician role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - #BiometricsSAS Programming, #Biostatistics, Data Management Tel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Join an inclusive and welcoming team.
At SEC we've cultivated an atmosphere where we encourage each other to perform, progress, and be successful. Join an organisation that puts their people at the heart of everything they do.
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You need a recruitment partner you can trust. Whether you're considering the next move in your career or need support executing your growth strategy, we can help.
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SEC prove time and time again that they are best in class. They are responsive, go the extra mile, are passionate about what they do and show they really do care and that it isn’t just about numbers. We recently requested some market research into rates, location and compliance, and they responded to our need within the hour. They are a friend in need (no, they really are!) when help is needed.
Hiring Manager
Global CRO
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SEC have supported us with through a critical biometrics project, and have excelled in producing quality candidates throughout our partnership. They are pleasure to work with, have a supportive and attentive team, and demonstrate a keen eye for detail. I'm continually impressed with the knowledge and expertise of the SEC consultants, I trust their judgement completely.
HR Manager, EMEA
Global CRO
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We get a lot of calls from staffing agencies but what I liked about SEC’s approach was that there was not unnecessary perseverance. The team has been very sensitive about ensuring that they are in contact with us when we need them to be. The team didn't over-sell themselves and let their work speak for itself – that's what's important to us when choosing a recruitment partner.
VP, Clinical and Regulatory
Medical Device Startup, USA
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Jacob Perrett May 2022
Four Massachusetts-based Cell and Gene Therapy start-ups that are taking 2022 by storm
The east coast of America is seeing a boom in the number of cell and gene therapy (CGT) start-ups setting up shop. In particular, Massachusetts has seen a real rise in the number and some of these have huge promise. Here is a list of four Massachusetts-based CGT start-ups that are already making an enormous impact on the industry and will continue to do so into the future. Dyno Therapeutics Dyno are a Cambridge based biotech who launched in May last year. Their work combines both AI and gene therapy to solve the challenges of in-vivo gene delivery. The AI-powered tech will improve the design of gene therapies by making them safer, more effective, and applicable to more diseases, heightening the potential to provide life-changing treatments for millions of patients In the coming years Dyno are going to be ones to watch, they secured $100 million in Series A funding upon their launch and have some impressive partnerships with the likes of Roche, Novartis, and Sarepta Therapeutics. They’ve gained a good amount of media attention ; this year they were named as one of America’s Best Startup Employers by Forbes, and named Emerging Company of the Year by the New England Venture Capital Association. With all of this under their belt, they’re sure to see an influx in prospective employee interest and a bright future ahead of them. Scorpion Therapeutics A Boston-based company, Scorpion Therapeutics launched in October 2020 with the aim to develop the next generation of targeted cancer therapies. The company are revolutionising the CGT cancer sector and pushing towards an “era of Precision Oncology 2.0” by building on the scientific breakthroughs of the past 20 years. What’s looking promising for Scorpion is their diverse and deep pipeline of optimized drug discovery programs which are being developed “at unparalleled speed and scale compared to existing benchmarks”. It’s clear that investors too can see the potential Scorpion have; when they first started out they received $108 million in Series A funding, fast forward 3 months and they’ve received a further $162 million in Series B funding. With an exciting pipeline and huge investments, Scorpion have piqued the interest of some of the pharma giants, entering an agreement with AstraZeneca back in January to discover, develop and commercialise novel cancer treatments against ‘undruggable’ targets. With so much buzz happening around the company, it’s likely Scorpion have all they need to secure a fruitful future. Ensoma After securing $70 million in Series A funding, Ensoma are another one to watch. They are just over a year old, launching in February 2021 in Boston, and have had a great first year. Ensoma engineer gene therapies that treat rare monogenic illnesses, and since launching they have developed the first in-vivo editing platform that precisely engineers hematopoietic and immune cells with a one-time, off-the-shelf treatment. This success to likely to continue due to the support from top-tier investors, along with Ensoma’s strategic collaboration with Takeda. This partnership has the potential for Ensoma to receive up to $1.25 billion from Takeda, assuming the programs are a success. Strand Therapeutics Another emerging biopharma is Strand Therapeutics. Located in Cambridge, MA, Strand are among those using synthetic biology and applying it to RNA therapeutics. The company launched in June 2021 and is co-founded by world-leading researchers from the MIT Synthetic Biology Center. With a cool $52 million in Series A funding, their technology has the potential to revolutionise CAR-T therapy while also being applicable across a broad spectrum of other diseases. At present Strand are developing the first platform for the creation of programmable, long-acting mRNA drugs which will be capable of delivering precise, multi-functional, potentially curative treatments with a single dose. With exciting prospects on the horizon, Strand Therapeutics are definitely going to be one to watch.
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Harvey Curzen May 2022
An insight into the challenges of cell and gene therapy commercialisation
Reaching the market with cell and gene therapies (CGTs) is no easy task. Despite there being over 1,000 ongoing clinical trials for cell and gene therapies, there are currently only 23 FDA approved CGTs on the market globally. This is not putting off investors though, roughly a third of all private investments made last year in the life sciences industry were within CGT: a whopping $68 billion. With such huge amounts of investment, it is easy to forget that we are currently in the early stages of CGTs commercialisation. Globally, there is a large eligible patient population who are ready and waiting to see the benefits of CGT but haven’t received the treatment yet. In the US for example, fewer than 20% of patients eligible for CAR-T therapy, a therapy used to recognise, target, and destroy cancer cells, are receiving it. Therefore, the commercialisation timeline needs to accelerate in a timely manner to help raise the statistics.So what are some of the hurdles faced when it comes to cell and gene therapy commercialisation?Target population sizesFirstly, CGTs are very expensive, and typically have small target markets. This makes them a tougher sell when it comes to governments and healthcare bodies; When a treatment can only help a relatively small number of patients, they’re more likely to be deemed unprofitable, and pose greater risk for those involved in purchasing decisions. In the case of Glybera, this is exactly what happened. Glybera was the world’s first gene therapy to receive approval in Europe, and due to commercial failure, the developers did not renew its market authorisation. The CGT was priced at €1 million, making it the most expensive treatment upon its commercialisation in 2012, and also had a small target market. This made it hard to convince governments to get behind it and continue to pay for it. Global healthcare infrastructureFor CGTs to help their target populations, the healthcare infrastructure will need to change at a global level. Currently, most hospitals do not have the facilities, processes, or expertise in place to provide patients with access to CGT treatments. With the amount of CGTs on the market growing at a relatively slow pace (only two were approved by the FDA in 2021), and as CGTs only help a small audience, it’s not likely that there will be a quick uptake in the healthcare industry making commercial success a challenge.Demand for talentTo support the uptake of CGTs, commercial directors need to have talented people on the ground and at the moment there is a shortage of qualified talent. One reason behind this is that, commercially speaking, CGT is a very new field. This means there are few people who have hands-on experience when it comes to leading a successful CGT commercial strategy, as it’s been done so few times. Hiring experienced commercial heads may therefore be a struggle for small or midsized companies, as many of the businesses that work within CGT and have the resources to attract and retain these people are larger companies. Following decades of effort to establish and progress the field, the future of personalised care, targeted treatment, and fights against rare disease are clearly looking more optimistic thanks to the capabilities shown by cell and gene therapies. It’s clear too, though, that transformation across the healthcare sector will need to be undertaken in order for us to see widespread commercial success, and to realise the full potential offered by CGTs.Harvey Curzen has vast knowledge and experience in the commercial space, specialising in cell and gene therapy within the DACH region. For support in securing your business-critical hires or to enquire about our open opportunities within the sector, connect with Harvey on LinkedIn here, or send him an email at harvey.curzen@seclifesciences.com.
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consultantstories
Olivia Skye May 2022My workplace non-negotiables: How I knew SEC was the right environment for me
I started my recruitment journey back in 2019, just shy of three years prior to joining SEC. I began my career working the EU and UK markets, but was drawn in by the hustle and bustle provided by the US market. I soon switched my remit and have been working with stateside clients and candidates ever since.When the opportunity came up to join the newly formed US division at SEC, it looked like the ideal opportunity - but it was going to take somewhere special for me to consider a new role.I joined SEC with the purpose of expanding our US life science presence. This was something I knew I could do and knew I could do well, as in my previous firm I’d built up the US market from scratch. So, when the chance to join SEC came up, the opportunity looked ideal for me.But when I was considering a new role there were three non-negotiables – things I’d consider dealbreakers if the agency I was interviewing with couldn’t offer them.First, homeworking flexibility was essential. When the pandemic hit, like so many of us, I had to adjust to working from home - and I came to love it. With the everyday commute too and from the office gone, I got back hours of my life that I didn’t even realise I was losing. With this new control over these hours I became so much more productive day-to-day, and knew that this was the way I wanted to work. "Having the flexibility to work from anywhere has allowed me to fulfil some of my life goals. I always wanted to live abroad, and SEC allowed me to do that."One of my biggest passions in life (second to life science recruitment, of course!) is to travel, and after 8 years in London I was ready for a change of scenery. As well as the flexibility to work from home, I knew I wanted to be with an agency that would allow me to work from anywhere. Once restrictions eased and international travel was possible again, I took my chance and upped and moved to Spain – and SEC were open to the fact I’d be working outside of the country. Being based here my hours are slightly different; I’m an hour ahead of the UK and 6 hours ahead of the US, so my work day starts at noon. It might not be everyone’s cup of tea, but I feel like I’m living my absolute dream lifestyle. Now before I start work, I have the time to go to the beach and workout, the freedom in my mornings is great. Then, at lunch I’ll go for a walk around my area, usually back to the beach (it’s just so close to my house) before working through until around 9pm. Spanish culture works so well with my hours, as unlike the UK, everyone tends to have dinner around 9-10pm anyway. So, I’ll have time to go out and meet my friends for dinner before starting all over again the next day. Having the flexibility to work remotely has allowed me to fulfil some of my life goals. Ahead of turning 30 I’d always wanted to live abroad, and SEC allowed me to do that. My second dealbreaker was relating to development. I wanted to constantly be learning, developing, and growing as a consultant. When I started at SEC I had just under three years of experience, and I knew that there were areas that I wanted to improve in. Since joining I’ve learnt a lot more than I ever anticipated I would, purely because of the experience the senior team have here. SEC recently brought on a new Performance and Development Director, Pin, and - no exaggerations - he is a legend. In the time that I’ve been here he has taught me so much already, things I didn’t realise I needed teaching or brushing up on. Everyone, no matter what position you are in, is seen and treated as equals. Even if you are an experienced recruiter, you’re not expected to know everything, and with the support here I’m learning every single day. It’s just been so refreshing. "When I joined SEC I had just under three years of experience, and I knew knew there were areas I wanted to improve in. Since joining I've learnt a lot more than I ever anticipated I would, purely because of the experience the senior team have here."And finally, I needed my potential manager’s leadership style to connect with how I like to be managed. When you first start, SEC ask their consultants to do a characteristics personality assessment. I loved this because its purpose is to clearly see how someone likes to learn, and which environments they like to work in and can thrive in. Based on this, the managers can adapt their style and approach to suit that individual. As an experienced recruiter finding a manager that takes this seriously, trusts you, and supports you in your role all while helping you build your desk is often hard to come by, especially working remotely. So, knowing that this assessment was in place, and after the initial conversations ahead of joining, it was clear that these were my kind of people. SEC recognised me as an individual and valued my recruitment skills, so coming in as an experienced consultant they were flexible in accommodating and supporting my career trajectory. The time and effort that my managers have put into my development has been next-level and I’m so appreciative of that. With this support, both my team and I have had some great successes, we’ve opened some fantastic clients, and so I am really excited to continue on my SEC journey.
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Clinical
Jacob Stafford-Wright May 2022Five biotech innovators transforming mental health care
A mental health crisis has sparked innovation from major names within the biotechnology industry, with several firms hitting the spotlight in the last few years as a result of cutting-edge research, contemporary methodology or innovative product application in the treatment of anxiety, depression, PTSD and other cognitive disorders.A particularly flourishing branch of mental health treatment can be seen in the use of psychedelics, where early research and application is garnering promising results, the likes of which haven’t gone unnoticed by major life science firms and investors alike.But the mental health market is massive, and it’s not only psychedelics drawing attention to the space. Wearables, diagnostics, artificial intelligence, and digital engagement platforms are all being explored with the intent to provide better outcomes for mental health patients. Here are five firms making waves in the sector.Lobe Sciences Lobe Sciences focus on the clinical development of medical devices and psychedelic medicines to treat neurological disorders and brain traumas, and have an impressive and diverse portfolio of 5 provisional patents – 3 for treatments that use psychedelic compounds and a further 2 for medical devices.Last year the firm announced a joint venture with Virtual Psychedelics Incorporated to develop digital therapeutic pods, set to be powered by a custom tech stack that combines display technology and biomonitoring to create a multi-sensory virtual experience."We believe this technology will be able to assist those suffering from depression, PTSD and other mental health issues. The KrysalisTM Pod is being designed as a therapeutic system capable of delivering an easy, immersive media experience, while simultaneously collecting critical biometric data in a safe and monitored environment."Sage TherapeuticsPostpartum (or postnatal) depression is believed to be the most common complication of childbirth, affecting roughly 1 in 7 people after delivering a child. Typically though, new mothers have had access to no treatments specifically designed to target the condition. Instead, they are prescribed antidepressant drugs that are approved for the general population, so it's not clear if they're safe or effective, and they don't always work.Sage Therapeutics set out to change this, and their treatment ZULRESSO became the first FDA-approved treatment for the condition back in 2019, and remains the only treatment specifically indicated for postpartum depression (PPD). In studies, mothers undergoing the treatment after childbirth experienced a reduction in symptoms of PPD in just 2.5 days, with maintained results in mood measured at the 30-day mark too.Last year the company planned to launch three new trials to test an additional product, SAGE-217, against the treatment of the condition.Neuronetics Commonly prescribed treatments for clinical depression often come with the risk of adverse side effects, so many patients opt against traditional antidepressant drugs. Neuronetics provide an alternative with their product NeuroStar, a non-drug, non-invasive treatment that uses magnetic pulses to stimulate areas of the brain that are underactive in those suffering from depression.An open-label trial into the product saw almost half of participants experience significant improvement in depression symptoms. Some also experienced an improvement in their anxiety, appetite, and energy levels.The market-leading medtech firm has delivered over 2.8 million treatments to patients suffering from depression since their product hit the market in 2008, and in 2020 they were named as a Top 10 Neurology Device Provider by MedTech Outlook Magazine.atai Life SciencesGlobal biotech atai Life Sciences have only been in the mental health space since 2018, but are involved in almost a dozen ongoing efforts analysing the effect of various compounds on depression, anxiety, addiction, and other mental health disorders.Many of the therapies under research by atai make use of psychedelic compounds, but since 2020 the company have also invested heavily in the digital health space, acquiring a majority stake in digital therapeutics firm Psyber and launched their own digital platform, IntroSpect.The company hope to utilise the flexibility and power of technology to meet the need of patients on their own terms, and use digital biomarkers to make mental health treatments more refined, effective and individualised.Pear TherapeuticsSince 2020, Pear Therapeutics has announced a variety of partnerships with key players in the fields of wearables, diagnostics and AI and between 2020 and 2021 raised $80m to develop their digital therapeutics that aim to support the treatment of a variety of cognitive disorders.They hope to redefine medicine by discovering, developing and delivering software-based therapeutics to provide better outcomes for sufferers of depression, bipolar disorder, schizophrenia and substance use disorder. Pear hit the news in 2021 as the Ohio Department of Mental Health & Addiction Services became the third state regulator to fund their digital therapeutics to tackle behavioural health and addiction recovery.
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consultantstories
Crystal Leung April 2022Motivation and Momentum: The road to placing my first candidate at SEC
I joined SEC back in July 2021. I had just moved from Canada in 2020 and was working in the retail and hospitality sector. Being in these kinds of roles meant that I was constantly talking to people, so this really honed my ability to communicate with strangers. Throughout my life I’ve always had a good work ethic, I’m constantly striving to achieve the best. So, when I first heard about recruitment, it really intrigued me. I realised my skills and what drives me could align with recruitment nicely, and so I really started to consider it as a career.When I first started I knew that recruitment wouldn’t be easy. Even though I felt I had a fair understanding of what a career in recruitment would look like, I knew a placement wouldn’t just fall into my lap and that it’d take a lot of groundwork to get a sale in the pipeline. To reap the rewards, I needed to put those months of effort in through making calls, sending emails, and getting to know people. My first placement was a Senior Project Manager of Regulatory Affairs in a contract research organisation (CRO). This kind of position isn’t one that myself or my team typically place; regulatory affairs isn’t usually our remit. But it worked out that when I came across this role, I had just come across this particular candidate and knew this could turn into something really great, the stars aligned you could say.Once I started working the role everything progressed quickly. That evening I was on the phone with candidates discussing what they were looking for and the position we had on offer. I’d had a couple of initial conversations with a great candidate that was working for an agency but felt like this line of work was limiting them and not opening a lot of doors for them, so right away I knew that career progression was going to be a huge motivator for them when considering an offer. The candidate and I really built up a strong level of trust, so I knew that they were in other hiring processes with different companies. What made them choose this role over the others was down to this trust. They knew I wanted the best for them, I wouldn’t put them forward in this role if it wasn’t 100% aligned with their motivations. In the end, they went with my client and were onboarded in the new year. Overall, with it being across the Christmas break and everyone slowing down, it was a 2 month process of interviews and daily communication. Even after they had accepted the position and weren’t due to start for a few weeks, I was still catching up with them on a biweekly basis just to make sure everything is sitting well with them and they’re still looking forward to joining. I feel like the crucial part of making my first placement was nailing down the candidate’s motivations straight away. Before this placement I had a couple of offers on the table which had unfortunately fallen through due to the candidates accepting counteroffers – a tough reality I know every recruiter faces. It was a total learning curve, and from it I realised that knowing and understanding your candidates’ motivations was vital in making sure you’re able to place them. It was such a good feeling when my candidate accepted the offer, it felt as though those first three months of training and hard graft had really paid off. For me, placing this candidate was the best motivator to keep pushing on, and keep striving for that next deal. After this I went on to join the US team, working in the analytical department and have been thriving since, I feel as though I’ve really found my niche. Now I’m already feeling like I’m a better recruiter, I’ve hit the ground running and I just need to keep it going, keep the momentum, and keep it moving. SEC’s training program really helped me to secure my first placement. Here I’ve got the tools to learn, the opportunity to progress, and freedom to build out my own remit. I’ve learnt so much since July and I can’t wait to see where I’ll be this time next year. Looking for a career in recruitment? Send your CV to us here and our talent team will be in touch.
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Employer Resources
Emma Hobbs March 2022In a market as competitive as life sciences, your employer brand is key to securing top talent
In today’s increasingly competitive life science market, many active candidates are juggling two or three processes when it comes down to offer stage, and the most in-demand passive candidates are approached by dozens of talent acquisition teams each month. With 75% of candidates looking into your reputation before they even consider applying to your vacancy, taking control over your identity as a workplace is one of the most effective ways of positively impacting your talent pipeline. In the job climate of 2022, it isn’t enough to advertise a role and expect your ideal candidate will apply. In fact, less than 1 in every 20 candidates we placed last year came from an inbound application as a result of us publicising a role. For the small number of candidates that do come in through active recruitment channels, they face more choice than ever before and often have multiple processes ongoing. Demand at an all-time high post-pandemic, more life science organisations are gaining the attention of investors and hitting the limelight, and employers are able to attract a wider pool of talent with the adoption of remote working - all of which make it more difficult for smaller organisations to attract talent.As a small to mid-sized organisation, your reputation as an employer of choice should be a consideration when it comes to growth strategy. Consistent messaging of what your workplace has to offer in terms of benefits, culture and opportunities is one of the most impactful ways of reaching that passive candidate goldmine. Effective messaging that taps into a candidate’s desires could be the difference between securing those ideal hires, or them accepting the offer of your competitor. What do candidates want to know? To understand where to start when it comes to your employer branding strategy, it’s important to know what employees today actually expect from their workplace. Passive candidates aren’t won over by the mission of a company, the type of clients you work with, even your place in the market – when considering a move, they want to know exactly what’s in it for them. Sent at the right time, messaging that speaks to candidate expectations doesn’t just support in attracting passive talent before they hit the job boards, but can also help in pre-closing any candidates you might have in process already. Earlier this year we surveyed more than 800 life science candidates and asked about their motivations when it comes to career moves. From a list of the most common employee value propositions (EVPs), the four that were most popular among our respondents were flexible working options, clear career progression, good work-life balance, and a competitive salary package (which came out on top, with 70% of candidates saying this was essential). Knowing what resonates with your ideal hires is key to constructing the right message, and these top desires are a good place to start. You can also uncover hidden facets of your current employer brand and what your candidates might expect by surveying your current employees, collecting feedback from candidates you’re interviewing, analysing data from exit interviews, and checking employment sites such as Glassdoor. Questions to answer when developing your employer brand.What does the company stand for?What benefits set us apart from our competitors?What makes the company unique?What do our current employees say about us?What makes ours a credible organisation?How do we keep on top of our employee's needs?What's our value proposition?Why should prospective hires care about us?How do you get the message out there? Employer branding is just one side of the coin – once you have a clear idea of the message you’d like to present, it’s time to begin recruitment marketing. The careers section of your company website is your shop window, and is important both as a dedicated channel for showcasing your workplace and a place to direct your audience with the intention of converting them to applicants. A dedicated careers page provides a good framework for measuring the success of your employer branding and recruitment marketing efforts, through traffic and conversions, which can be done through a tool such as Google Analytics. You should also consider how you could alter the content you already use when undergoing a recruitment drive, such as reformatting your job adverts to put your culture and benefits front-and-centre instead of touching only upon the vacancy requirements itself. When it comes to external messaging, think about where your candidates spend most of their time and consider ways of involving your business in the conversation. One of the most popular and cost-effective channels for employers to showcase what they have to offer is on the company social media channels, particularly LinkedIn, the world’s leading online professional networking channel. With the help of your marketing function (if your organisation has one) consider how you might build regular and consistent messaging of your EVPs into your existing social content calendar to reach the passive talent networks that are on the platform. Company channels aside, tapping into the networks of your employees has the potential to increase your reach tenfold. The top way people discover new job opportunities is through referrals, and influencer marketing techniques tell us that people are more likely to trust a recommendation when it’s coming from an individual compared to a business entity. Effective use of this powerful resource can allow your existing team to populate your talent pipeline. Consistency is the most important factor when it comes to building an impactful and sustainable employer brand, and with any marketing activity you’re unlikely to see meaningful results overnight. For guidance on how you can reach your ideal candidates, devise the right message to market, stand out against your competitors, and gain an advantage when it comes to attracting top life science talent to your organisation, reach out to our client services team here, or connect with me directly on LinkedIn.
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Clinical
Jacob Stafford-Wright March 2022International Women's Day 2022: Four life science pioneers shaping modern medicine
March 8th marks International Women's Day, and this year the theme is #BreaktheBias. Since 2015 the number of women graduating in core STEM subjects in the UK has grown from 22,000 to almost 25,000, but in 2021 females still only made up 26% of those graduating in STEM subjects, and just 24% of the average STEM workforce – this figure drops to as low as 10% for some industries. With the #BreaktheBias theme in mind, we wanted to recognise the critical role women play in STEM industries through celebrating four pioneers within the life science industry that are transforming the medical landscape through leadership and technical innovation. Carolyn Yarina, CEO and Co-Founder of Sisu Global HealthWhen a patient suffers internal bleeding, surgeons have two options; reach for a blood bag, or recycle the patient’s own blood using a process called autotransfusion. In many developing countries, though, lack of access to blood banks or a lack of blood donorship might mean the surgeon doesn’t have access to a blood bag, and the technology typically used for autotransfusion is expensive and requires power – a commodity not always available in emerging markets. After founding a non-profit that supported mobile clinics in India, Carolyn went on to co-found Sisu Global Health, a company focused on the research, development and commercialisation of medical devices aimed at emerging markets. The Sisu-developed Hemafuse, a handheld medical device that replaces the need for donor blood by recycling a person’s own from internal bleeding, launched in Ethiopia, Kenya and Ghana in 2020. Allysa Dittmar, President and Co-Founder of ClearMask With over 95% of those living with hearing loss saying masks and facial coverings impact their ability to communicate, Allysa, who has been deaf herself since birth, set out to design a transparent mask with her fellow public health students at Johns Hopkins University and co-founded ClearMask LLC. Allysa and the team at ClearMask have developed the first FDA-approved transparent face mask, allowing for the deaf and hard of hearing that would usually rely on lipreading for communication to do so clearly, without the obstruction a standard face mask would cause.Dr. Crystal Icenhour, PhD, CEO and Co-Founder of Aperiomics A rising star of American biotechnology, Dr. Crystal Icenhour holds two patents, has authored and co-authored numerous scientific publications and is a prolific speaker at many scientific conferences. In 2014 she co-founded Aperiomics, a bioinformatics firm that uses advanced data analysis and next-generation sequencing technology for detecting infectious disease. Where traditional infection testing might look at one bacteria, fungus or virus at a time, DNA sequencing technology developed by Dr. Crystal’s firm can identify every known pathogen there is – that’s nearly 40,000 microorganisms – from within a single blood sample. It’s the mission of the infectious disease firm to transform infection testing, and leverage the power of technology to advance human life and quality of life. Dr. Kimberly Smith, MD, MPH, Head of R&D at ViiV Healthcare Dr. Kimberly Smith heads up research and development at the only company wholly dedicated to HIV therapies, ViiV Healthcare. During her time at ViiV Dr. Kimberly has launched more than 25 late-stage trials for seven new medicines, and is working to revolutionise the management of HIV through regimes that decrease the lifetime exposure to medicines by suffers of HIV. Since working on the frontline of the AIDS epidemic as a clinician in the 1980s, Dr. Kimberly has made it her life work to answer the unmet needs of those living with the illness, and has been a public advocate for female and PoC representation in STEM professions and in exec level roles.
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consultantstories
Holly Hermance February 2022Full circle: The journey from Consultant to Associate Director
Danny has been involved in life science recruitment since 2012 with experience in both permanent and contract hiring. He joined SEC as associate director in October 2021 and has been heading up the contract team since. In that time alone, Danny has grown his contract team from six to ten, and has ambitious plans for further headcount growth. We sat down to talk to him about his first few months at SEC and to learn more about his plans for the future.So this isn’t exactly a welcome, but a welcome back! What made now the right time to return to TeamSEC?That’s right! My first ever recruitment role was actually at SEC way back in 2001. I started at consultant level and stayed for a while before leaving to pursue my own business, but I’ve kept a close eye on SEC since. Now, after 20-plus years of experience in the industry, I’m back again as associate director. Not to sound too cliché, but it really does feel as though I’ve come full circle! SEC is kind of like a sleeping giant, in that it has a great reputation but has never reached its full potential. I came back to help in executing an ambitious 5-year plan, push out this “sleeping giant” notion and help the contract function and wider business become a go-to life science firm, globally. The notion of what was on the horizon here was a huge draw for me to come back. When I looked at SEC’s growth plans together with my experience and skillset, I knew I was the one for the job. In my previous workplace I developed my team into 360 consultants. With that, when I left, my team were the top performing team in the business. That’s what made me excited about this role, I knew I could do exactly the same here, I’m starting fresh. Give us a bit more information on your role, and what you’re aiming to achieve as associate director.I’ve been brought on to grow and scale the contract side of SEC across multiple divisions. I’m going to be growing my team, not just in headcount, but growing the quality of my team, the businesses we work with and calibre of candidates we represent. We’ve invested heavily in our L&D recently, so my plan is to really utilise this and take the team all the way to the top. I’m not saying that my team are going to be the biggest or the best contract team in the life sciences sector, or even in London, that’s immeasurable. But what I do want is for my team to be recognised as a successful one, a knowledgeable one, one that people want to work with and one that other recruiters want to be in. My aim is the same with our clients and candidates; I want them to engage with SEC as their number one supplier. You mention the five-year plan in place - what’s going to keep that momentum going for you as we progress through this growth period?The team. The team I’ve inherited here, as well as the wider team I’m collaborating with too, is a really good one. They have the qualities that nowadays are difficult to find: enthusiasm, the want to do a good job, the pace, the thunder, the willingness to listen, and the willingness to learn. They’re open to change, open to learning, and for me those kinds of people are the ones I want to teach and mentor. We have a range of consultants in my team from veteran recruiters who’ve been around the block to our early talent who are so hungry to make their mark. The people we have now provide an ideal blueprint for the kind of recruiters we want to join us and share in this journey. That’s so exciting for me. What are the core priorities for us this year?Our people are the core priority this year. We want to solidify our early talent and get them to be the best consultants possible. At the same time, we want to make sure we have the right people in the right seats. By this I mean getting the best talent out there to come into this business while also nurturing the early talent. We’ve invested heavily in L&D to create our own talent, but also to help elevate our experienced consultants. We want both our senior consultants and newer consultants to have constant learning and development opportunities so they can grow and achieve their goals. It’s in place right now with the Future Leaders Programme and Early Talent Development Academy, but it’s only going to develop and grow as we do. It’s only been six months since you joined, but are there any success stories or core highlights you could tell us about?My team have given me so many things to be proud of. One of the biggest things was when a member of my contract team did his first 360 deal. When I took over the team, he’d expressed to me that he really wanted to do a 360 deal but was tentative as to whether he could do the BD necessary to get there. But the attitude and energy that he has saw him push on, believe in himself, and complete his first 360 deal. I honestly felt like a proud dad! At the start of 2022 my team also saw three double promotions. In my 20 plus years of recruitment I know this is a rarity. For it to happen in my own team not once but three times was something I won’t forget. The amount of hard work and dedication my team put in is second to none. I’ve found that in this job you can teach skill, and you can teach the recruitment process, but the willingness to get out of bed and do a good day’s work can’t be taught, it comes from within, and the team have that naturally. And finally, what would be your top tips for someone who was looking to join #TeamSEC?My advice is to always have a clear goal. When I look back over my career that’s probably when my performance wavered – when I wasn’t focused. When I had a clear goal, I achieved exactly what I wanted to every single time without fail. No matter your age, recruitment experience, or personal circumstances, having a strong focus and a clear why about what you are doing will set you up for success.
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Holly Hermance January 2022
Has the pandemic changed the perception of the pharmaceutical industry?
Despite being an industry that serves the general population, the pharmaceutical industry has always polarised public opinion, faced antitrust scrutiny and had business practice continually under fire. Now, with the effort against Covid-19 dominating headlines for close to two years, pharmaceutical companies have now become household names. Unsurprisingly, as more people become aware of these firms, the stronger an opinion forms on the industry. Pre-pandemic, the UK public perception of the pharmaceutical sector was dubious with the pharma industry scoring just 44 on the 2019 Edelman Trust Barometer, a reputation calculator, putting them in the untrusted category. The UK aren’t alone in having poor public perception of the pharma market, public in the US also had a negative attitude towards the pharmaceutical industry. According to Gallup’s 2019 report, the pharma industry was ranked worst when it came to Americans’ views of the sector, unseating the US federal government as the lowest rated industry that year (which it had held since 2011).Two years later, and there has been somewhat of a shift in attitudes towards the pharmaceutical sector, as an industry-wide effort to eradicate coronavirus has focused public attention on the effort the sector goes to in the name of public health. Now, recent studies by the Pew Research Center and Wissenschaft im Dialog have shown a significant increase in public trust of the pharma industry, most notably in Germany and the US, and it’s looking as though that perception is at a net positive globally, too - a recent APCO Worldwide survey found that 52% of respondents now have a more positive perception towards the industry than before the pandemic began.The sector’s response to the COVID-19 pandemic has had a huge impact on public perception. The APCO Worldwide survey, conducted 8 months before the first COVID-19 vaccine was approved in the UK, found that 68% of respondents were optimistic that the pharmaceutical industry would develop a treatment for COVID-19.Professionals within the industry have also noticed the change in attitude, with Eva Prieschl-Grassauer, Chief Scientific Officer at Austrian respiratory and allergy company Marinomed, crediting the shift in attitude to the sector’s “fast reaction to the pandemic and focus on the development of vaccines”. Some believe this newfound positive public perception will last. The CEO and co-founder of a Swiss-German cancer immunotherapy firm VAXIMM, Heinz Lubenau, states that the industry has demonstrated its value to both health care systems and the economy, anticipating that the appreciation will last. “In the light of the mutations, competition for effective medicines will continue and public awareness of the biotech sector will be maintained".But some question the durability of this buzz. Shahar Silbershatz, CEO of reputational analytics company Caliber, states that the “attention afforded by the COVID-19 pandemic offers a once-in-a-generation opportunity to emphasise [the pharmaceutical industry’s] importance and potentially repair their reputation”, but warns it also could be their downfall if not handled correctly. With the rapid speed of bringing a COVID-19 vaccine to market, people may now expect that ‘miracle’ treatments or vaccines will come out for other illnesses just as fast - this leaves a high potential for disappointment and could prove to be reputationally harmful. The pandemic has affected both those who have had the virus and those who have not. The speed that the pharmaceutical industry, regulatory bodies and governments worldwide have dealt with the virus helped to deliver vaccines in record time and save many lives, which could be enough to ensure this new-found appreciation and confidence in the industry is here to stay.
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TeamSEC
Jacob Stafford-Wright January 2022The stories behind the scholars: hear from two graduates of the SEC Scholars Programme
Last year, and in partnership with In2ScienceUK, we launched the SEC Scholars initiative; a 5-year programme that will provide at least 50 young people with guidance, mentorship, and practical skills to support their journey towards a career in STEM. Last summer we supported 11 students through the programme – here are the stories of two of our recent graduates. Barriers faced when pursuing a career in STEM contribute to the fact that less than 10% of all life science professionals in the UK come from working-class backgrounds. They pose a threat to upward mobility within the sector, contribute toward under-representation, and negatively impact diversity and the talent pipeline the country has to offer. For more than 10 years In2ScienceUK have been working to provide young people from low-income and other disadvantaged backgrounds with the resources needed to tackle such barriers, starting with assistance in preparing for and entering university. Last year we launched a long-term partnership to support in their mission to open STEM opportunities up to everyone. The Programme GraduatesAspiring research scientist, Sejal Sejal applied for the programme to expand her knowledge of chemistry and explore the potential roles that would be available to her when embarking on a career in STEM. As part of the programme, Sejal worked with a mentor from within the industry and had the opportunity to conduct research, present her work and pose questions about careers in the field directly to a research scientist. “The programme helped me develop transferable skills that will benefit me in the future but has also confirmed my aspiration in pursuing a STEM-related career. Attending the research lectures and completing the set tasks enabled me to develop critical and analytical thinking skills as well as improve my communication skills through the discussion boards and social hubs. The programme has helped enhance my confidence in learning a STEM subject.” Currently in year 13, upon completing her A-levels Sejal is looking to enter university and pursue a Master of Chemistry degree with the aspiration of entering a career as a research scientist. Biomedical science enthusiast, Mohamed Mohamed was hoping to pursue a degree in biomedical science, and attended a placement day in a biomedical research institute as part of the programme last summer alongside his mentor, a scientist working in the field. Mohamed also attended research courses and workshops to give him a well-rounded picture of what a career in biomedical science could offer. “For me, the best part of the whole experience was the placement day I attended at the Francis Crick Institute. I got to actually meet real scientists and people that have degrees in the things I want to get into. The day itself was split into two parts; first I met with lots of people that worked at the Institute who told us about their journey to how they became what they are. After that, I got to take part in lots of hands-on activities with some of the scientists.” Originally apprehensive about constructing his university application, the programme offered Mohamed support in putting together a strong personal statement and improving his writing skills. Mohamed’s appetite to pursue biomedical science was strengthened as a result of attending the programme, and he credits his mentor, a scientist, on providing a positive perception of what it means to be a professional in the field and work in a real-life laboratory setting. You can read more about the work of In2ScienceUK over on their website. More information about last year’s programme can be found in their 2021 Impact Report.
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