Biometrics

Biometrics

EPM Scientific:

Specialist Talent Partner in Biometrics & Bioinformatics Recruitment

Data collection, analysis, and real-time oversight are key factors in clinical research and trials that lead to health innovations in medical technology and pharmaceutical industries. It is impossible to demonstrate human intervention effectiveness in trials, estimate side effect prevalence, evaluate diagnostic procedures, or prove scientific hypotheses without Biometrics.

With data being at the forefront of ongoing research, development, and trials, the demand for trained bioinformatics, biostatisticians, and other biometrics professionals is increasing. In 2021, the global healthcare biometrics market size was valued at US$26.02 billion. This figure is expected to grow at a CAGR of 18.1% from 2022-2030 to a staggering US$79 billion. The job market is already fiercely competitive, and finding the right talent for Biometrics roles can be challenging. EPM Scientific is here to source the right candidates for jobs in this field.

How we can help

Since 2012, EPM Scientific has been the preferred talent partner of major life sciences companies globally. Our ability to source rare talent for clinical trial and research roles in Biometrics and place the best candidates quickly and precisely comes down to our investment in best-in-class technologies and in our talent experts’ development. EPM Scientific supports you every step of the way as we find the best opportunities for you.

Biometrics talent solutions

EPM Scientific provides contract, permanent, and multi-hire Biometrics talent solutions from our hubs around the world. We offer retained and contingent services bespoke to your company’s hiring needs. Our permanent talent solutions alongside our extensive contractor and interim manager networks allow us to place the right people in the right roles. We make relevant recommendations and manage the process from source to hire, using our consultative approach.

EPM Scientific is Phaidon International’s specialist life sciences brand. Our global team offers value creation services and high-level account management.

Don’t just take our word for it 

“Working on our behalf as an external recruiting vendor, EPM Scientific found us a very good Biostatistician candidate, and provided us a positive client experience.” – Max Minowitz, Head of Talent, Santen 

“I’d say EPM Scientific are a great support for our recruiting efforts at Vanda! We receive good candidates in a timely manner for our open requisitions even if they are niche positions.” – Alec Tausch, Human Resources Senior Associate, Vanda Pharmaceuticals


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How we can help

Since 2012, EPM Scientific has been the preferred talent partner of major life sciences companies globally. Our ability to source rare talent for clinical trial and research roles in Biometrics and place the best candidates quickly and precisely comes down to our investment in best-in-class technologies and in our talent experts’ development. EPM Scientific supports you every step of the way as we find the best opportunities for you.

Benefits of working with us

Experience

We have over a decade’s worth of experience as a leading talent partner in Life Sciences & Pharma.

Network

A vast, global network of the best, in-demand professionals, working with the world’s largest Life Sciences institutions, to take drugs, devices and therapeutic applications through from conception to completion.

Knowledge

Our award-winning talent specialists offer bespoke, tailored guidance on the latest hiring trends and industry news to help you achieve your goals.

Looking to hire?

Data collection, analysis, and real-time oversight are key factors in clinical research and trials that lead to health innovations in medical technology and pharmaceutical industries. It is impossible to demonstrate human intervention effectiveness in trials, estimate side effect prevalence, evaluate diagnostic procedures, or prove scientific hypotheses without Biometrics.

With data being at the forefront of ongoing research, development, and trials, the demand for trained bioinformatics, biostatisticians, and other biometrics professionals is increasing. In 2021, the global healthcare biometrics market size was valued atUS$26.02 billion. This figure is expected to grow at a CAGR of 18.1% from 2022-2030 to a staggering US$79 billion. The job market is already fiercely competitive, and finding the right talent for clinical research biometrics roles can be challenging. EPM Scientific is here to source the right candidates for jobs in this field.

Biometrics Jobs

As a leading talent partner, EPM Scientific sources talent for diverse Biometrics roles. Some of the top roles include Statistical Programmers, Biostatistician and Associate Directors.

Snr Director Statistical Programming

We have a current opportunity for a Snr Director Statistical Programming on a permanent basis. The position will be based in California or Massachusetts. For further information about this position please apply. Job Title: Senior Director of Statistical Programming Salary: $230,000-$260,000 base Position Overview: We are seeking an experienced and highly motivated Senior Director of Statistical Programming to lead our statistical programming team. This role is critical to our clinical development efforts and will involve overseeing the design, development, and implementation of statistical programming activities for our clinical trials. Key Responsibilities: Lead and manage the statistical programming team, providing mentorship and guidance to junior programmers. Oversee the development, validation, and maintenance of SAS programs to support clinical trial data analysis and reporting. Collaborate with biostatisticians, data managers, and clinical teams to ensure the accuracy and integrity of clinical trial data. Develop and implement standard operating procedures (SOPs) for statistical programming activities. Ensure compliance with regulatory requirements and industry standards (e.g., CDISC, FDA, EMA). Participate in the preparation of statistical analysis plans (SAPs) and clinical study reports (CSRs). Provide strategic input on statistical programming aspects of clinical development plans. Stay current with industry trends and advancements in statistical programming methodologies. Qualifications: Advanced degree (Master's or Ph.D.) in Statistics, Mathematics, Biostatistics, Computer Science, or a related field. Minimum of 14 years of experience in statistical programming within the biotech or pharmaceutical industry. Proven leadership experience with a track record of managing and developing high-performing teams. Expertise in SAS programming and familiarity with other statistical software (e.g., R, Python) is a plus. Early and late stage clinical trial experience Regulatory interraction experience Strong knowledge of clinical trial design, data management, and regulatory requirements. Excellent problem-solving skills and attention to detail. Strong communication and interpersonal skills, with the ability to work effectively in a collaborative team environment. What We Offer: Competitive salary and benefits package. Opportunity to work in a fast-paced, innovative environment. Career growth and development opportunities. A supportive and inclusive company culture.

US$230000 - US$260000 per year
United States of America
Apply

Manager/AD Standards Statistical Programming

We have a current opportunity for a Manager/AD Standards Statistical Programming Role on a permanent basis. For further information about this position please apply and let's have an open discussion. Job Title: Manager/Associate Director, Statistical Programming Standards Job Type: Full-Time Department: Biostatistics and Programming Job Summary: We are seeking an experienced Manager/Associate Director of Statistical Standards Programming to join our dynamic team. The successful candidate will be responsible for developing and maintaining programming standards, ensuring compliance with regulatory requirements, and providing expertise in R and SAS programming. This role will involve collaboration with cross-functional teams to support clinical trials and other research activities. Key Responsibilities: Develop, implement, and maintain statistical programming standards and guidelines. Ensure compliance with regulatory requirements and industry best practices. Provide expertise in both R and SAS programming to support clinical trial data analysis and reporting. Collaborate with biostatisticians, data managers, and other stakeholders to ensure the quality and consistency of statistical programming deliverables. Lead the development and maintenance of standard macros, templates, and tools to improve efficiency and quality. Provide technical leadership for statistical standards Accountable for utilizing statistical methods for data analysis, providng R Packaging Review and approve programming deliverables to ensure adherence to standards. Stay current with industry trends and advancements in statistical programming and regulatory requirements. Qualifications: Bachelor's or Master's degree in Statistics, Computer Science, or a related field. Minimum of 5 years of experience in statistical programming within the pharmaceutical or biotechnology industry. Clinical trial experience in early/late stages Expertise in both R and SAS programming languages. Strong knowledge of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., CDISC). Excellent problem-solving skills and attention to detail. Strong communication and interpersonal skills. Ability to work effectively in a team-oriented environment. Experience with clinical trial data and ICH/CDASH/CDISC standards (SDTM, ADaM, TFL) is highly desirable. Preferred Qualifications: Master's in Statistics, Computer Science, or a related field. Experience in a leadership role within statistical programming. Knowledge in other statistical programming languages/software like Spotfire, WinBUGS, Python, , etc Benefits: Competitive salary and benefits package. Opportunities for professional development and career advancement. Collaborative and inclusive work environment.

US$140000 - US$180000 per year
United States of America
Apply

Clinical Operations Statistician

**Clinical Operations Statistician - Contract Role in Europe** Are you a seasoned Clinical Operations Statistician looking for your next challenge? We are on the hunt for an individual with exceptional expertise and a minimum of 10 year's experience within late phase or phase 4 studies. This is a freelance, contract position where you will play an integral role dedicated to a sponsor, supporting performance by monitoring the clinical research organisations work load (CROs) through pivotal stages such as data base lock and ensuring secure storage of critical trial data. Key Responsibilities: - Work closely with CRO staff to prepare databases for locks - Handle complex statistical analyses during various study phases - Manage the organisation and long-term storage of clinical trial data Required Skills: - **Late Phase/Phase 4 Studies Expertise:** Your extensive background working on later stage trials provides assurance that our high standards can be met. - **Data Base Lock Proficiency:** You'll bring proven ability to support teams up until database lock-an essential milestone marking readiness for regulatory submission. - **Bio-statistics Knowledge:** As standard practice dictates, being well-acquainted with bio-statistical methods puts forth efficiency when dealing with intricate data sets. This opportunity requires someone based anywhere across Europe who relishes freelancing flexibility while engaging deeply within their field. If this speaks directly to your professional aspirations, we invite applications from those prepared to elevate operations statistics into new realms of excellence within pharmaceuticals and clinical trials sectors.

Negotiable
Netherlands
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Director of Biostatistics

Position Summary: The Director of Biostatistics will play a critical role in the design, analysis, and interpretation of clinical trials. This individual will provide strategic leadership and expertise in biostatistics to support our Phase III clinical programs. The ideal candidate will have a strong background in biostatistics, experience in CNS clinical trials, and a passion for innovative research. Key Responsibilities: Lead the biostatistics function for Phase III clinical trials, ensuring robust statistical design and analysis. Collaborate with cross-functional teams, including clinical development, regulatory affairs, and data management, to develop and execute statistical analysis plans. Provide statistical input into clinical trial protocols, study design, and regulatory submissions. Oversee the preparation of statistical sections of clinical study reports, regulatory documents, and publications. Ensure compliance with regulatory guidelines and industry standards for statistical practices. Mentor and develop junior biostatisticians, fostering a culture of continuous learning and innovation. Stay current with advancements in biostatistics and clinical trial methodologies, applying best practices to our research programs. Qualifications: Ph.D. or Master's degree in Biostatistics, Statistics, or a related field. Minimum of 10 years of experience in biostatistics, with a focus on CNS clinical trials. Proven track record of leading biostatistics efforts for Phase III clinical trials. Strong knowledge of regulatory requirements and guidelines for clinical trials. Excellent communication and leadership skills, with the ability to work effectively in a collaborative team environment. Proficiency in statistical software (e.g., SAS, R) and clinical trial data management systems.

US$220000 - US$230000 per year
Pennsylvania
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Sr. Director of Clinical Data Management

Sr. Director Clinical Data Management San Diego, CA - Hybrid 198,000-286,000 A leading biotech company, based in San Diego, is advancing its first two programs into the clinic this year. Their advanced drug discovery platform uses cutting-edge technology to design highly targeted cancer therapies. This innovative approach aims to create precise treatments with improved efficacy and reduced side effects, driving their mission to revolutionize cancer care .Backed by over $200 million in funding from top-tier investors, the company is well-positioned for rapid growth. The leadership team includes an award-winning CEO recognized for entrepreneurial excellence and a CMO with a distinguished track record in precision medicine and immunotherapy. Joining this company means contributing to innovative cancer treatments within a dynamic, well-funded environment alongside passionate experts committed to transforming oncology. The Senior Director of Clinical Data Management Responsibilities will include: Leading clinical data management oversight of clinical trials, including project management, CRO management, coordination of internal reviews, and approval of routine data management deliverables. Setting up data management vendors as required, including the review of RFPs, evaluating, and negotiating data management budgets and contracts. Leading the development and review of all Clinical Data Management-related documents, including Data Management Plans, CRF design and CRF Completion Guidelines, edit check specifications, data transfer plans, etc. Liaising with study management CRO and internal cross-functional teams to ensure adequate site training, timely initiation, and overall data integrity. Providing direction and guidance to team members, including consultants and vendors, as well as other cross-functional groups to achieve study goals and milestones. Overseeing database design and post-production updates, ensuring that CROs, vendors, and internal staff meet the highest quality standards per the latest industry standards and regulatory requirements. Being responsible for sponsor user acceptance testing, including documenting findings and resolving issues with CRO. Overseeing data management activities, including reconciliation between external data and EDC data, data flow metrics, database migration, medical coding, and driving data snapshot/closeout activities. Proactively identifying risks and executing risk mitigation strategies; maintaining timely communication with both upper management and cross-functional teams. Supervising CRO/Vendor activities to ensure GCP compliance, quality expectations are met, and timelines are adhered to. Contributing to program deliverable timeline creation and project re-forecasting. Supporting data management activities for regulatory submissions. Leading the development of CDM-related Standard Operating Procedures (SOPs) and Work Instructions. Performing additional duties as assigned. Qualifications Bachelor's degree mandatory, with a minimum of 6years hands-on data management experience in the CRO, biotech, or pharmaceutical sector. Oncology experience required. Strong vendor management skills

US$198000 - US$286000 per year
San Diego
Apply

Director, Clinical Data Management

Job Title: Director, Clinical Data Management (CDM) Location: New York Job Summary: The Director of Clinical Data Management (CDM) will assist with leading the CDM team in the design, implementation, and management of clinical data systems and processes. This role is responsible for ensuring the accuracy, integrity, and security of clinical trial data. Key Responsibilities: Develop and implement data management strategies and processes for clinical trials. Ensure the accuracy, integrity, and security of clinical trial data. Oversee the development and execution of data management plans, including data collection, cleaning, and validation. Ensure compliance with regulatory requirements and industry standards (e.g., FDA, ICH-GCP). Qualifications: Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred. Minimum of 8 years of experience in clinical data management Strong knowledge of clinical trial processes and regulatory requirements. Excellent leadership, communication, and interpersonal skills. Strong problem-solving skills. Preferred Qualifications: Knowledge of programming languages (e.g., SAS, SQL).

US$170000 - US$180000 per year
New York
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Director, Clinical Data Management

Job Title: Director, Clinical Data Management (CDM) Location: New York Job Summary: The Director of Clinical Data Management (CDM) will assist with leading the CDM team in the design, implementation, and management of clinical data systems and processes. This role is responsible for ensuring the accuracy, integrity, and security of clinical trial data. Key Responsibilities: Develop and implement data management strategies and processes for clinical trials. Ensure the accuracy, integrity, and security of clinical trial data. Oversee the development and execution of data management plans, including data collection, cleaning, and validation. Ensure compliance with regulatory requirements and industry standards (e.g., FDA, ICH-GCP). Qualifications: Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred. Minimum of 8 years of experience in clinical data management Strong knowledge of clinical trial processes and regulatory requirements. Excellent leadership, communication, and interpersonal skills. Strong problem-solving skills. Preferred Qualifications: Knowledge of programming languages (e.g., SAS, SQL).

US$170000 - US$180000 per year
New York
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AD Statistics Late Stage Oncology

Job Title: Associate Director, Biostatistics Late Stage (Oncology) Salary: $180k-220k base + bonus + benefits Job Summary: The Associate Director of Biostatistics in Oncology will provide strategic and technical leadership in the design, analysis, and interpretation of clinical trials in oncology. This role will collaborate with cross-functional teams to ensure the statistical integrity and scientific validity of clinical studies. The Associate Director will also contribute to regulatory submissions and the development of innovative statistical methodologies. Key Responsibilities: Lead the statistical design and analysis of oncology clinical trials, ensuring robust and scientifically sound methodologies. Collaborate with clinical development, regulatory affairs, and other departments to develop clinical trial protocols and statistical analysis plans. Provide statistical expertise for regulatory submissions, including preparation of statistical sections of INDs, NDAs, and other regulatory documents. Oversee the development and validation of statistical models and methodologies for oncology studies. Ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and Standard Operating Procedures (SOPs). Review and approve statistical deliverables, including analysis datasets, tables, listings, and figures. Participate in the selection and management of biostatistics vendors and contractors. Stay current with advancements in statistical methodologies with oncology late stage research, incorporating new techniques as appropriate. Present statistical findings to internal and external stakeholders, including regulatory agencies and scientific conferences. Qualifications: Ph.D. or Master's degree in biostatistics, statistics, or a related field. Minimum of 5 years of experience in biostatistics, with at least 3 years in a Study/Project leadership role within oncology late stage expertise. Vendor Management Oversight experience Strong knowledge of clinical trial design, statistical analysis, and regulatory requirements in oncology. Proficiency in statistical software (e.g., SAS, R) Excellent organizational, communication, and leadership skills. Ability to work collaboratively in a fast-paced, dynamic environment. Detail-oriented with strong problem-solving and analytical skills. Preferred Qualifications: Experience with global clinical trials and regulatory submissions (FDA, EMA) Knowledge of CDISC standards (SDTM, ADaM). Experience with adaptive trial designs and Bayesian methodologies.

US$180000 - US$220000 per year
Basking Ridge
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Sr. Director of Clinical Data Management

Sr. Director Clinical Data Management San Diego, CA - Hybrid 198,000-286,000 A leading biotech company, based in San Diego, is advancing its first two programs into the clinic this year. Their advanced drug discovery platform uses cutting-edge technology to design highly targeted cancer therapies. This innovative approach aims to create precise treatments with improved efficacy and reduced side effects, driving their mission to revolutionize cancer care .Backed by over $200 million in funding from top-tier investors, the company is well-positioned for rapid growth. The leadership team includes an award-winning CEO recognized for entrepreneurial excellence and a CMO with a distinguished track record in precision medicine and immunotherapy. Joining this company means contributing to innovative cancer treatments within a dynamic, well-funded environment alongside passionate experts committed to transforming oncology. The Senior Director of Clinical Data Management Responsibilities will include: Leading clinical data management oversight of clinical trials, including project management, CRO management, coordination of internal reviews, and approval of routine data management deliverables. Setting up data management vendors as required, including the review of RFPs, evaluating, and negotiating data management budgets and contracts. Leading the development and review of all Clinical Data Management-related documents, including Data Management Plans, CRF design and CRF Completion Guidelines, edit check specifications, data transfer plans, etc. Liaising with study management CRO and internal cross-functional teams to ensure adequate site training, timely initiation, and overall data integrity. Providing direction and guidance to team members, including consultants and vendors, as well as other cross-functional groups to achieve study goals and milestones. Overseeing database design and post-production updates, ensuring that CROs, vendors, and internal staff meet the highest quality standards per the latest industry standards and regulatory requirements. Being responsible for sponsor user acceptance testing, including documenting findings and resolving issues with CRO. Overseeing data management activities, including reconciliation between external data and EDC data, data flow metrics, database migration, medical coding, and driving data snapshot/closeout activities. Proactively identifying risks and executing risk mitigation strategies; maintaining timely communication with both upper management and cross-functional teams. Supervising CRO/Vendor activities to ensure GCP compliance, quality expectations are met, and timelines are adhered to. Contributing to program deliverable timeline creation and project re-forecasting. Supporting data management activities for regulatory submissions. Leading the development of CDM-related Standard Operating Procedures (SOPs) and Work Instructions. Performing additional duties as assigned. Qualifications Bachelor's degree mandatory, with a minimum of 6years hands-on data management experience in the CRO, biotech, or pharmaceutical sector. Oncology experience required. Strong vendor management skills

US$198000 - US$286000 per year
San Diego
Apply

Sr. Clinical Data Manager

Sr. Clinical Data Manager San Diego, CA - Hybrid $220,000-$286,000 A leading biotech company, based in San Diego, is advancing its first two programs into the clinic this year. Their advanced drug discovery platform uses cutting-edge technology to design highly targeted cancer therapies. This innovative approach aims to create precise treatments with improved efficacy and reduced side effects, driving their mission to revolutionize cancer care .Backed by over $200 million in funding from top-tier investors, the company is well-positioned for rapid growth. The leadership team includes an award-winning CEO recognized for entrepreneurial excellence and a CMO with a distinguished track record in precision medicine and immunotherapy. Joining this company means contributing to innovative cancer treatments within a dynamic, well-funded environment alongside passionate experts committed to transforming oncology. The Senior Director of Clinical Data Management Responsibilities will include: Leading clinical data management oversight of clinical trials, including project management, CRO management, coordination of internal reviews, and approval of routine data management deliverables. Setting up data management vendors as required, including the review of RFPs, evaluating, and negotiating data management budgets and contracts. Leading the development and review of all Clinical Data Management-related documents, including Data Management Plans, CRF design and CRF Completion Guidelines, edit check specifications, data transfer plans, etc. Liaising with study management CRO and internal cross-functional teams to ensure adequate site training, timely initiation, and overall data integrity. Providing direction and guidance to team members, including consultants and vendors, as well as other cross-functional groups to achieve study goals and milestones. Overseeing database design and post-production updates, ensuring that CROs, vendors, and internal staff meet the highest quality standards per the latest industry standards and regulatory requirements. Being responsible for sponsor user acceptance testing, including documenting findings and resolving issues with CRO. Overseeing data management activities, including reconciliation between external data and EDC data, data flow metrics, database migration, medical coding, and driving data snapshot/closeout activities. Proactively identifying risks and executing risk mitigation strategies; maintaining timely communication with both upper management and cross-functional teams. Supervising CRO/Vendor activities to ensure GCP compliance, quality expectations are met, and timelines are adhered to. Contributing to program deliverable timeline creation and project re-forecasting. Supporting data management activities for regulatory submissions. Leading the development of CDM-related Standard Operating Procedures (SOPs) and Work Instructions. Performing additional duties as assigned. Qualifications Bachelor's degree mandatory, with a minimum of 6years hands-on data management experience in the CRO, biotech, or pharmaceutical sector. Oncology experience required. Strong vendor management skills

US$220000 - US$286000 per year
San Diego
Apply

Senior Biostatistician

Senior Biostatistician We are seeking an experienced and highly skilled Senior Biostatistician to join our client's growing Biostatistics team. In this role, you will play a key part in the design, analysis, and interpretation of clinical trial data across a variety of therapeutic areas. You will work closely with cross-functional teams to ensure high-quality statistical methods are applied to clinical research, contributing to the advancement of innovative medical treatments. Key Responsibilities: Lead the statistical design and analysis of clinical trials, ensuring compliance with regulatory requirements and industry standards. Collaborate with clinical teams to interpret data, provide insights, and support decision-making throughout the trial lifecycle. Develop statistical analysis plans (SAPs) and perform complex statistical analyses using a range of methodologies. Communicate statistical results clearly and effectively to both technical and non-technical stakeholders. Mentor junior statisticians and provide guidance on statistical best practices. Qualifications: PhD in Biostatistics, Statistics, or a related field. Extensive experience in statistical analysis, with a strong background in clinical trials and regulatory submissions. Proficiency in statistical software such as SAS, R, or other relevant tools. Strong communication and collaboration skills, with the ability to work across teams and present findings to diverse audiences.

US$120000 - US$140000 per year
United States of America
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Biometrics News & Insights

How to Write a Job Description for a Biostatistics Role Image
Highlights

How to Write a Job Description for a Biostatistics Role

​Finding the right individual for a Biostatistics role in your life sciences company can be challenging. Get the process off to a good start by writing a clear and accurate job description for the role.A well-crafted job description for a Biostatistics role can help you to:Filter applicants by allowing professionals to assess their fitness for the role.Determine vital Key Performance Indicators(KPIs) for job evaluations during post-hire probation.Mitigate legal risk by ensuring employee- and employer-alignment regarding job expectations such as usual duties, responsibilities, and tasks, as well as regularization metrics.In this article, EPM Scientific sheds light on how to write an effective job description for a Biostatistics role.Writing a Biostatistics job descriptionA Biostatistics job description should contain a few key elements to be effective. These include responsibilities, skills, qualifications, remuneration (if possible), benefits, company information, and the company’s core values.Remember to be specific by defining the role’s purpose, include objectives such as KPIs used to measure success, describe the activities involved and the results desired, ensure the role’s overall goals are realistic, and include the role’s time-bound goals.Main responsibilities of a BiostatisticianIndividuals in Biostatistician roles, particularly in senior positions, provide a wide variety of guidance, support, and advanced statistical knowledge to faculties, managers, researchers, and scientists. Additionally, they participate in the design, development, and reporting of studies and trials, and they collect, analyze, and interpret data across multiple entities, responding to a range of complex statistical issues in life sciences research settings. Some of the main responsibilities to include in a job description (if applicable to the role at your company) are:Designing, analyzing, implementing, and reporting findings on targeted studiesProviding consulting to researchers and investigatorsWorking with investigators on analysis plan formalization and reporting specificationsReviewing and monitoring biomarker analysis, safety reporting, and other aspects of clinical trial monitoringAssisting with the preparation of protocols, investigator brochures, clinical trial documents, peer-reviewed manuscripts, scientific abstracts, and regulatory agency request responsesServing as subject matter expert for committees, research teams, and other collaboratorsOverseeing and coordinating statistical support staff, data entry staff, and others on an operational basis or on a project or site.Important skills and qualifications required for a senior positionA good job description for a Biostatistician role should include an overview of the key skills and qualifications that your company is looking for in a candidate in a senior position. In addition to the relevant academic and training qualifications, these skills should include:Knowledge and understanding of scientific approach and methodologies, principles, concepts, methods, and standards of statistical researchAbility to apply advanced techniques in support of research studies and experimentsAbility to analyze, interpret, and draw conclusions from complex informationAbility to provide leadership and technical guidance to professionalsStrong time management skills, ability to prioritize, analytical communication, problem-solving skills, and critical thinkingShowcasing your companyCreating a good job description for a Biostatistics role gives you an opportunity to showcase your company. By describing your company culture and offering a clear idea of a day in the life of someone in the role, it can inspire suitable candidates to take action.In addition to portraying the type of person who will flourish in your company, a good job description can be used to market your company to potential candidates, and to highlight your employer value proposition. Ensure you provide an overview of your company’s mission, culture, values, and benefits, as well as what makes your company appealing and unique.Hire for a senior Biostatistics role with EPM ScientificThere is no need to struggle with finding the right people for senior Biostatistician roles at your company. Partner with EPM Scientific and let us pair you with the perfect talent. Submit a vacancy or request a call back now.

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biometrics

Life Sciences Salary Guides of 2023

Are you aiming to advance your career within the life sciences sector? Are you interested in discovering your competitors‘ offerings for professionals in your field across the APAC region? We are excited to present our new series of Salary Guides for the life sciences industry. These comprehensive reports will furnish you with invaluable insights into the present salary trends in Singapore, China, Australia, South Korea, and Japan.Compiled from the responses of almost 900 life sciences professionals in the APAC region, this is an opportunity you shouldn't overlook. Seize the chance to gain a competitive advantage in the life sciences field, enabling you to make well-informed choices about your career trajectory, compensation, and hiring approaches.

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The Life Sciences Skills Gap: How to Hire Image
management advice

The Life Sciences Skills Gap: How to Hire

​The life sciences industry is rapidly growing, but it is experiencing skills gaps that need to be addressed to allow it to reach its full potential. According to a 2022 life sciences and pharma talent trends report, 33% of C-suite and human capital leaders in the life sciences and pharmaceuticals sector agree that talent scarcity is a major pain point. This problem is widespread, with the UK also suffering a skills shortage that threatens to stall the industry’s trajectory.Skills gaps in digital and computational skills, and industrial, economic, and clinical research are particularly large. However, if phenotypic, genomic, and patient data integration practices can be optimized across the industry, this will support both research and treatment advances in the future.This article shares effective hiring strategies that can help life sciences organizations address skill gaps within their teams and wider business.Understanding the skills gaps in the life sciences industryStatistics from the talent trends report highlight the key skills gaps in the life sciences industry and how they impact key research and development processes. Demand for life sciences products is forecast to grow more rapidly than the global GDP over the coming years, and 45% of the aforementioned talent leaders note that they are looking to hire primarily to avoid talent scarcity from hindering their organizations’ progress. Moreover, the report found that 67% of pharmaceutical and life sciences companies believe that reskilling their current employees is an efficient way to address and mitigate skills gaps. It currently takes 105 days on average to fill a non-executive life sciences position in the US, leading to financial losses of $500 per open role per day, so intentional talent strategies are crucial to setting life sciences businesses on the path to success.Supporting mobility between sectorsSupporting mobility between sectors plays a vital role in closing the skills gaps within the life sciences industry. Enabling professionals to transition across sectors, ranging from Regulatory and Legal Services to Pharmaceutical and Medical Device Engineering, allows life sciences companies to tap into a vast pool of talent. This is also an effective method of sharing intersectional knowledge and developing key skills.Selecting candidates with a diverse range of backgrounds for open roles may also bring more unique perspectives into your organization, thereby driving innovation and helping to meet growing demand. Focus on transferable skillsFocusing on transferable skills is a powerful approach to bridging the skills gap in the life sciences industry. Rather than solely emphasizing sector-specific experience, prioritizing transferable skills enables professionals to adapt and thrive in new roles within the field. The life sciences industry’s talent offers a myriad of transferable skills that can be used to power future growth and innovation. These include analytical skills, leadership and teamwork skills, problem solving, written and oral communication skills, management skills, and scientific peer communication. Additional soft skills to focus on in your talent acquisition strategy include critical thinking, problem solving, and attention to detail.Consider cultural fitSeek out candidates from other industries who align with your organization’s culture, values, and core mission. This alignment promotes employee engagement, retention, and overall job satisfaction, whilst creating a supportive working environment that benefits from a wide range of experiences and perspectives.These candidates should also possess the aforementioned transferable skills, which will help to ensure that they can perform optimally in their new roles without being hindered by common skills gaps.Offer more flexibilityWhile not a priority for all candidates, flexible working arrangements such as remote or hybrid work arrangements are valuable to skilled candidates and may help to give your organization an advantage in the ongoing competition for life sciences talent.Hire top talent with EPM ScientificEPM Scientific is a leading specialist life sciences talent partner, providing you with a wealth of expertise to help you locate the best talent for your life sciences roles globally. Submit a vacancy or request a call back from our team to find the right people to drive your organization forwards.

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clinical-development

Interview & Hiring Guidance

​5 essential tips for employers, hiring managers, and HR on the hiring process in Life SciencesThe interview process, from initial phone call screenings and psychometric testing, to face to face interviews with the hiring manager and onsite tours, can often be a long and laborious process. So it is imperative to keep an interview process streamlined and engaged, to ensure talent doesn’t drop out, and your organization, and yourself is represented best. Here are 5 vital top tips for employers to stick to when interviewing top talent. Be present Showing excitement to prospective candidates provides insights for them into the potential team culture and attitude. Asking them questions about themselves, on their interests, their lives, their careers, as opposed to only technical questions to vet their hard skills, goes a long way in connecting on a human level. Another way to connect is by sharing real life examples of the day to day, positive experiences about the role and team, and details about project work. These are important talking points candidates like to know, and while they understand an interview may be rigorous technically, maintaining the conversational, human aspect is important too. Being engaged may sound simple, but given how much of the interview process is over Zoom/VC/phone these days, it is easy to get distracted and check emails or open windows on your computer. Remaining attentive and interested will bring the best out of the interview process and provide a positive candidate experience. Also important is to be interesting yourself. Be in sell modeMany of the above points are indirect examples of selling your team and role. However, in a more overt way, providing exciting opportunities at present and for future career growth are always on candidates’ minds and knowing there is more to be excited about than just hands-on skills or what is in the job description on day one makes them buy into the role and organization more. As part of selling the role, explain why you took this position, and what you liked about the company and team. Be relatable to their circumstances and share with them why the position in your team, at your company, is the best move they can make.Another important aspect to highlight here is the culture. Maybe there is more to what makes the role great than just the daily tasks or responsibilities, such as company sports team, lunch clubs, charitable groups, or environmental initiatives. Highlight what else is enjoyable so that candidates are excited about this role, as well as the team and company, aside from the day to day. These days competition for top talent is so tight, that those cultural differences can distinguish you amongst the rest.Be positive Many of the above points translate to this aspect of hiring, but above all, being cordial, professional, and sharing timely feedback all contribute to a positive candidate experience. In some cases, the candidate may not be a good fit culturally, or for your position, but you should still offer them professionalism and positivity in the interview. Remember, they may have colleagues or a network of other experts that could be better suited for your role/team. You want them to have a positive experience to refer people to you, and maintain your company’s reputation in the market, as well as your own. It's also important to note that many candidates often have other processes in the mix, so if you give them any chances to doubt their experience, they could be more likely to go elsewhere. Be flexible If a professional isn’t the 100% right fit, still ask yourself if there is a place for them in the team or organization, especially if they bring something unique to the company. Keep an open mind when recruiting talent, and consider the future headcount. Potentially you can create a new role for an exceptional candidate, especially if you don’t want to lose someone good to a competitor. See the positives in a candidate’s skillset if they bring enough to the table, and find reasons to say yes, especially in this market. Outside of being flexible with the job description, can you also be flexible with the offer? Offering nuanced benefits, flexible working, and customizing offers to the individual joining can again make the difference between rejecting and accepting. Be decisive The market is still exceptionally hot, so it is vital hiring managers are mindful of how quick an interview process needs to be. “Keeping someone warm” is so important, but if you can’t commit to them you do risk them going in another direction. Therefore, be timely with your feedback, especially if it's positive, to keep the momentum up. If they are at the top of your mind, you should stay at the top of theirs. Try and push approvals quickly as well. This is often bureaucratic but affect whatever influence you can have on an interview or hiring process, and don’t allow things to slow down if you can control it.Finally, be competitive. Don’t allow back and forth negotiations to hinder a process or allow time for other processes to catch up. Put your best, most competitive offer forward so it entices them from the very start.  To hire the best candidate for your open role, get in touch with EPM Scientific today. As a specialist talent partner in Life Sciences, we have access to industry-leading talent around the world. Find the talent you need by submitting your vacancy, or request a call back below to elevate your hiring process with the right talent partner today.

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How to Ensure Employee Retention in Life Sciences Image
safety-pharmacovigilance

How to Ensure Employee Retention in Life Sciences

​The Pharmaceutical market has expanded considerably in the past two decades, with Pharma revenues totalling $1.42tn in 2021. This has been accompanied by a growing demand for experienced, highly qualified Life Sciences professionals: with more drugs than ever now available, companies require a strong workforce to bring their products to market. The industry has had to deal with an ever-small talent pool as a result, which has been exacerbated by one of the highest employee churn rates, with the Life Sciences and Medical Devices industry alone seeing a 20.6% turnover rate. This is reflected in the results of our Life Sciences survey which revealed that more than 40% of Life Sciences professionals are currently looking for a new role.The COVID-19 pandemic led to a substantial increase in resignations across all industries, as many employees started to re-evaluate their priorities and seek roles that offered flexible remote-work policies. Consequently, companies have found it harder to get the people they need. 47.8 million workers in the U.S. decided to quit their jobs in 2021 – the highest volume of resignations since the Bureau of Labor Statistics began recording this data in 2001. This is equivalent to 3.98 million workers quitting their jobs each month, up from an average of roughly 3m leaving their jobs each month in 2019.Similar trends have been observed in Australia and the UK, where the rate of employed people between 16-64 choosing to switch jobs reached an all-time high of 3.2% between October-December 2021. The resignation rate continued to increase in 2022, with job-to-job resignations in the UK peaking at 442,000 in the second quarter of 2022. In Europe, one in three workers are considering quitting their jobs in the near term, with inadequate compensation and lack of career advancement being cited as the top factors.Why are Life Sciences professionals leaving their roles?The reasons that Life Sciences professionals have for wanting to leave their jobs vary across each industry sector. However, the promise of higher remuneration is invariably the main reason. This is according to findings from our Year in Review, which goes into greater depth about the factors that matter most to Life Sciences professionals when seeking to advance their careers.There are a host of other important factors, however, such as the desire for an improved work-life balance and employees wanting to acquire more new skills that will aid in their professional development. Changes in management can also cause people to want to move jobs, and Life Sciences professionals are increasingly looking for openings that provide flexible working hours and the ability to work from home.How to improve employee retentionThe good news is that there is a wide range of employee retention strategies that you can adopt in your workplace. Let’s take a look at some of the most effective employee retention techniques that you can use to ensure that your employees are satisfied at work and remain highly motivated in their positions, as opposed to looking elsewhere for their big career break.Offer competitive salaries and benefitsDissatisfaction around salary has had a negative impact on talent retention in the Life Sciences sector. As we’ve seen across the board, wanting higher compensation is the top reason for employees wanting to move to jobs; 70% of the R&D professionals that we surveyed within the Pharmacological industry were motivated by the promise of higher compensation at other companies.Paying your team a competitive rate is a simple but effective employee retention strategy that you can use to avoid your workforce shrinking. Our survey results show that the majority of respondents want a pay rise upwards of 10-15% of their current salary, which provides some indication of how much you may need to offer in order to remain competitive. Focus on career developmentYour employees will be far less likely to want to continue working for you long-term if there are few opportunities for advancement – or if their ability to develop their skills is limited. A study by Work Institute found that employees quit in 20% of cases due to career development issues.This highlights the importance of setting clear paths for career progression to give your team the motivation and provide them with long-term goals.Be flexibleOffering flexible working arrangements is a sure-fire way to keep your employees happy. Our Year in Review revealed that the option to work from home is very important to 60% of the industry as a whole. The majority of R&D respondents deemed flexibility as either important or very important, and workers in Pharmacovigilance ranked flexibility higher than salary when asked what is most important when considering a new job.Whilst a lack of flexible working options will not be a deal-breaker for many employees, you will find it far easier to retain your top talent if you grant them greater freedom to work according to their preferences.Build a supportive company cultureThere’s nothing quite like a warm, friendly culture when it comes to getting excellent work out of your employees. It’s also one of the best ways to increase their loyalty to the company.Seeking feedback from employees on a regular basis about how working processes might be improved helps ensure that workers feel that their concerns are being heard and addressed. Providing senior employees with the skills and training that they need to be good managers is also a worthwhile endeavour. Manufacturing professionals regard good leadership as almost as important as salary, according to our Year in Review survey.Promote work-life balanceMore than a third of respondents in our Life Sciences Year in Review report highlighted a poor work-life balance as one of the main reasons for wanting to seek employment in another role. Almost half of the Clinical Pharmacology professionals surveyed cited a need for an improved work-life balance as their main reason for seeking a new position.With higher numbers of professionals re-evaluating their priorities in life in the wake of the COVID pandemic, it’s no wonder that Life Sciences professionals are seeking out positions that allow them to spend more time with their families and friends. Giving your employees more personal time is therefore one of the most effective strategies for employee retention.Offer innovative, up-to-date technologiesFinally, ensure that you have the latest technology in your workplace. Investing in top-of-the-range software, for example, will make it easier for your employees to complete tasks and reduce the errors that are made, thereby increasing company productivity and boosting morale.Employee retention is critical to successThriving companies are characterized by a happy, satisfied workforce and high employee retention rates. Partner with EPM Scientific, a leading executive search firm for the Life Sciences industry, to find out more about how you can implement employee retention strategies that get results. Request a call back and one of our specialist consultants will be in touch. ​

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Pharmacology

Benefits of Life Sciences Contract Work

According to Statista, 86.5 million people in the United States alone will be freelancing by 2027, which is more than half of the country’s workforce – and this is a trend that’s not limited to the US. In Europe, it’s estimated that there are already 32.3 million freelancers making up 15% of the total labor market.If you’re in the Life Sciences sector, you can enjoy the benefits of contract work. The big question is, would a contract job be the right choice for you? This is an important question especially if you’ve built your career in permanent roles. Consider the benefits of being a contract employee and weigh them up against your own priorities to be better able to make an informed decision.The benefit of higher payHigher pay is one of the benefits of contract work. There’s a misconception that Life Sciences contractors do not earn as much as those in permanent roles, but the reality is that most Life Science companies are often willing to pay contract workers more money.  One of the reasons for this is that those companies do not have to cover health benefits, social security taxes, 401K (retirement) contributions, unemployment compensation, or Medicare for contract workers. They also understand that they need to compensate for the lack of company benefits and a steady income, especially if those contractors have a high level of expertise in their field.Freedom of choiceThe freedom to choose who you work with, where you work, and for how long you work is another of the benefits of contract jobs. As a contractor, you can carefully select the Life Sciences companies you want to work for, and you can choose roles or projects that interest you and avoid those that don’t. In addition, you can select the contracts that best suit you, whether you consider the location in which you will be based or the length of the contract.Gaining broad skills and experienceThe potential to gain much broader skillsets and a wealth of experience is another benefit of contract work in the Life Sciences sector. Making this benefit even more attractive is that you can do this in a relatively short time.As a contractor, you probably will fill a specific role for a variety of Life Sciences companies. By working on different projects in those companies, you will gain insights into and experience in a diversity of systems and workflows, some of which will be unique to specific companies. This is not possible if you remain a permanent employee within one company.Contract work also keeps work experience fresh, as your responsibilities are not likely to become monotonous or repetitive. The continued challenges that come your way are opportunities to diversify your skillset, which will count in your favor as you continue to progress your career through contract jobs. Find the right roleSince 2012, EPM Scientific has placed candidates in their next Life Sciences role, including both contract and permanent positions. Register your resume on our site to access the latest role​s on the Life Sciences job market and find out how we can help you define your next career move.​

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biometrics

Best Biometrics Team: In-House or Outsourced?

​Up to 77% of biotech and pharma outsource portions of their analytics or production. There are many reasons to outsource, in source, or stay completely in-house. For biometrics teams, outsourcing can increase standardization while staying in-house decreases turnaround time.Biotech and pharma often debate whether to outsource analytics. Benefits of outsourcing can include reduced costs, better standardization, or access to specialized equipment. Benefits of staying in-house include increased control and security. Some companies also choose to insource, hiring specialized teams for rapid turnaround times or skills transmission.  In this context, biometrics teams are no different from other specialized teams. Let's examine why…Benefits of an outsourced teamThe US has an estimated 50,000 vendors of contract analytical services and a 2016 study estimated 77% of biotech and pharma companies routinely outsource. The contract industry includes contract research organizations (CROs), contract manufacturing organizations (CMO) and contract development and manufacturing organizations (CDMOs). Collectively, the drug-discovery outsourcing industry is projected to reach $43.7 billion by 2026. Companies may choose to outsource for several reasons:Increased freedom: Analysis can be expensed instead of purching analytical equipment for experimental projects.Cost reduction: Project costs can be reduced up to 20% when overhead is taken into accountReduced risk: By restricting rigid costs from capital investments (i.e. real estate and lab equipment) companies can maximize variable costs (i.e. researchers and experimental projects)Benefits of an in-house teamOutsourcing is often better for small or mid-sized companies than large ones. When large pharmaceutical companies weigh in reasons not to outsource they most often cite the term “control.” This means mitigating risk by keeping critical supply-chain steps in-house and keeping confidential compounds out of settings who might also be serving a competitor.Some companies do insourcing instead, they have the equipment and supplies and hire specialized teams on a contract basis to achieve a rapid turnaround time, skills transmission, or scientific collaboration.  Outsourcing vs. insourcing for biometrics teamsBiometrics is the science of rapidly identifying individuals by physiologic or behavioral traits and it is used to obtain clean data for clinical trials.  Biometrics contractors tout data-integrity, reliability, and study-design as a reason to outsource biometrics. Certainly wearables,genomics,  and other novel identifiable methods of data collection involve specialized skill sets which may be more beneficial or cost-effective to outsource. However large companies may choose to retain control of personally identifiable information such as location data from wearables or genomic information used in clinical trials. We conclude that biometrics teams are like other specialized teams on the drug-development pipeline. Outsourcing will still become a cost-benefit analysis. Companies will have to individually decide how to strike a balance between control vs cost-reduction when it comes to outsourcing. In conclusionThere are pros and cons to outsourcing and insourcing. Individual companies must perform their own analysis to maximize their security while minimizing risk and expense.A good recruiter can make the difference for a company that is on the fence about these processes, or changing directions. Whether you are looking to find a good contractor or to shift from outsourcing to an in-house team EPM Scientific can help.EPM Scientific has a strong presence in both the US and abroad.  We ensure the best talent is in the right place at the right time to help promising products reach the market. Our process is fast, safe, and efficient.  If you are a US or international biotech company considering creating an in-house team or hiring an outside contractor with vetted KPIs, let us help you find the right connections. To be connected with a specialist recruiter, get in touch today.---------------------------------EPM Scientific is a leading specialist recruitment agency for the Life Sciences industry. We were founded in 2012 to give companies and candidates peace of mind that the recruitment process is in experts hands. Today, we provide contingency, retained search and project-based contract recruitment from our global hubs in London, Berlin, Switzerland, New York and Chicago.We pride ourselves in keeping our professional network up-to-date with any changes that will shape the future of work or affect the hiring process. Visit our website to discover more invaluable insights, including exclusive research, salary guides and market trends.

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