R&D

R&D

EPM Scientific: Specialist Talent Partner in Research & Development (R&D)Recruitment

Research and Development (R&D) transforms ideas into innovations in pharmaceuticals, biosimilars, medical technologies, and other healthcare. In 2023, 91% of life sciences organizations planned to invest in R&D innovation, with almost 50% of those organizations being optimistic about the sector’s outlook in 2024.

However, there are challenges in meeting the increased demand for R&D professionals. Overcome those challenges with EPM Scientific. As a preferred talent partner of industry leaders and promising startups, we will find and deliver the best people when your company needs them.

How we can help

We have sourced and delivered top Research & Development talent to companies and for over 10 years. Thanks to the ongoing investment in our talent specialists, premium technologies, and extensive professional network, we can meet your unique R&D talent needs with speed and precision. Let us find the brightest individuals or teams for oversight, managerial and other roles, or exciting career-furthering opportunities for you.

R&D talent solutions

EPM Scientific offers permanent, contract, and multi-hire R&D talent solutions tailored to your company’s requirements. We will work with you to understand who your ideal candidate is and then find the right person for the job, placing them timeously and smoothly. We also boast an extensive contractor and interim manager network for time-critical and long-term functions. Additionally, we offer bespoke retained and contingent services.

As well as finding and delivering top talent, EPM Scientific, part of Phaidon International, also specializes in offering high-level account management, and providing value adding services such as bespoke analysis and interviewing and hiring tips.

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Benefits of working with us

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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.

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Looking to hire?

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R&D Jobs

The R&D sector offers endless opportunities across seniority levels and specialisms, such as biochemistry and translational science. Some of the roles we hire for include Global Clinical Development Medical Director and Bioanalytical Chemist.

Senior Scientists (Analytical Development) - Cell Based Assays

Job Title: Senior Scientist, Cell-Based Assays Location: San Francisco, California Company: They are an innovative biotechnology company dedicated to advancing the field of Gene and Cell Therapy. Their mission is to develop groundbreaking therapies that improve the lives of patients worldwide. They are driven by a commitment to scientific excellence, collaboration, and innovation. Position Overview: They are seeking a highly skilled and motivated Senior Scientist with extensive experience in cell-based assays to join their dynamic research team. The successful candidate will play a critical role in the development and implementation of cell-based assays to support their drug discovery and development programs. Key Responsibilities: Design, develop, and optimize cell-based assays to evaluate the efficacy, potency, and mechanism of action of therapeutic candidates. Perform high-throughput screening and validation of compounds using cell-based assays. Analyze and interpret complex data sets, and present findings to cross-functional teams. Collaborate with other scientists and departments to integrate cell-based assay data into broader research and development efforts. Maintain detailed and accurate records of experimental procedures and results. Stay current with advancements in cell-based assay technologies and methodologies. Mentor and train junior scientists and research associates. Qualifications: Ph.D. in Cell Biology, Molecular Biology, Biochemistry, or a related field with 5+ years of relevant experience; or M.S. with 8+ years of relevant experience. Proven expertise in designing and conducting cell-based assays, including but not limited to viability, proliferation, cytotoxicity, and reporter gene assays. Experience with high-throughput screening and automation technologies. Strong analytical skills and proficiency in data analysis software (e.g., GraphPad Prism, Excel). Excellent problem-solving abilities and attention to detail. Strong communication and presentation skills. Ability to work independently and collaboratively in a fast-paced, multidisciplinary environment. Preferred Qualifications: Experience in the pharmaceutical or biotechnology industry. Knowledge of regulatory requirements and guidelines for cell-based assays. Familiarity with CRISPR/Cas9 gene editing and other advanced molecular biology techniques. Benefits: Competitive salary and benefits package. Opportunities for professional development and career advancement. Collaborative and inclusive work environment. Access to state-of-the-art facilities and resources.

US$140000 - US$180000 per year
San Francisco
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Associate Director Radiopharmaceutical Development-

Associate Director, Radiopharmaceutical Process Development Our client is a pioneering biotechnology firm specializing in the development of cutting-edge radiopharmaceutical therapies. Their rapid growth is fueled by a robust pipeline of successful projects and strategic investments. They are seeking an Associate Director of Radiopharmaceutical Process Development to drive the CMC radiopharmaceutical process development for all novel clinical programs. The Associate Director will execute the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product. In this role, you will translate pre-clinical/research methods and data to develop cGMP compliant processes and clinical drug product specifications, manage the execution of CMC studies, and author drug substance/product IND sections. Additionally, you will provide technical support and assessment to clinical manufacturing, including root cause analysis, change control, and process optimization. This role will serve as the main liaison between Tech Ops and research as well as the CDMO development team. Principal Responsibilities Process Development of Radiopharmaceutical Drug Product (DP) Lead the process development of radiopharmaceuticals for phase 1 clinical trials with a multidisciplinary team. Participate in the selection team to review RFPs, assess technical fit, and select the appropriate CDMO for development and manufacturing of novel products. Develop DP from DC selection to IND submission, including creating technology transfer packages, defining and managing development timelines, designing studies to determine suitable process conditions, and leading process qualification and validation campaigns. Write relevant CMC sections and supporting reports for regulatory submissions. Execute clinical readiness activities to enable clinical manufacturing. Technical Support of Clinical Manufacturing Provide technical direction to external CDMOs to draft manufacturing documentation. Partner with Quality to review manufacturing data and identify opportunities for risk reduction and continuous improvement. Support Quality/Regulatory assessments, including batch release, change control, deviations, OOs, and CAPAs. Liaison Between Research/Pre-Clinical and CMC Support the setup and ongoing function of the radiochemistry laboratory. Act as the liaison to partner with research radiochemistry and in vivo teams to share best practices and facilitate knowledge exchange. Qualifications, Education & Experience MSc or PhD in scientific fields with 10+ years of experience in the pharmaceutical industry, including radiopharmaceuticals. Knowledge of cGMP requirements, aseptic processes, and equipment qualification. Experience in writing CMC sections of regulatory submissions and clinical development and manufacturing. Experience with antibodies and bioconjugation is a plus. Good understanding of radiation regulations and guidelines preferred. Skills and Abilities Strong understanding of cGMP and FDA regulations. Excellent written and verbal communication skills. Strong analytical capabilities and critical thinking skills. Ability to troubleshoot complex problems and build rapport with all levels of the organization. Team-oriented, innovative thinker who enjoys a fast-paced, multidisciplinary environment.

US$160000 - US$200000 per year
San Francisco
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Director/Senior Director, Analytical Development

Director/Senior Director, Analytical Operations About The Job We are seeking an exceptional leader to develop and implement innovative analytical technologies and testing strategies from preclinical and IND-enabling studies through clinical development and commercialization. Who We Are We are an early-stage biotechnology company pioneering a new class of medicines for individuals, especially children, living with genetically driven diseases. Powered by a non-viral DNA vector system, our mission is to develop novel therapeutics that bypass the current limitations of gene therapy and achieve higher standards for potency, durability, redosability, and safety. Funded by leading investors and led by seasoned experts in gene delivery, protein sciences, and clinical translation. The Impact You Will Make This leader will be responsible for driving analytical technology innovation and development strategies for non-viral DNA-based gene therapy drug products, along with fostering a culture of inclusion, empowerment, scientific excellence, collaboration, and engagement. You will create a comprehensive roadmap for product analytics, contribute to long-term technology and operational strategies, drive rapid implementation of new technologies, and ensure functional excellence for regulatory strategies and operational efficiencies leveraging automation and state-of-the-art data management. This is a leadership position with critical accountabilities and influence on the pipeline product portfolio from pre-candidate nomination through research, development, commercialization, and beyond. The position requires strong technical partnership and collaboration with multiple stakeholders including Early Research, Gene Delivery Technology, CMC and Process Development, and Quality. This role is based in Southern California. What You'll Bring Technical Demonstrate technical leadership while collaborating closely with leaders from other functional areas and potential external partners. Serve as a thought leader for analytical technology innovation, integrated process and analytical control strategies, and integrated technical development and regulatory strategies for DNA-based vectors and non-viral DNA delivery technologies. Create a comprehensive roadmap for drug product and DNA vector analytics, as well as critical raw materials, process, and product residuals. Drive rapid implementation of new analytical technologies into CMC and clinical programs, ensure functional excellence for regulatory strategies for INDs and BLAs, and ensure operational efficiencies leveraging automation as well as state-of-the-art data analysis and management. Provide key strategic compliance and analytical development input to projects and cross-functional teams, including early research, and process development and manufacturing. Ensure scientific integrity and quality of regulatory submissions and support interactions with the global health authorities. Contribute Program Development Strategy including risk identification and mitigation plans, program development activities, timelines, and resource allocation. Leadership Build and strengthen a cohesive and motivated department that understands its issues, challenges, and opportunities. Engage and retain talent by understanding individuals' development needs and aligning with business requirements. As part of the R&D Leadership Team, drive technical vision, strategy, and programs to meet corporate objectives. As part of the R&D Leadership Team, help define and effectively communicate a compelling scientific vision internally and externally. As part of the R&D Leadership Team, contribute to gene therapy insights and technology through publications and external partnerships to deliver best-in-class therapies to patients. Education and Experience Required MS/Ph.D. degree in Immunology, Life Sciences, Chemistry, Pharmacology, or Engineering or similar. 5 years (>10 years for Senior Director) of experience in the development of gene therapy products or biologics. Knowledge and direct experience in developing analytical technology and methods, characterization and release of gene therapy drug products, including lipid nanoparticle (LNP) and/or polymer nanoparticle (PNP) formulation, is strongly desired. Experience with regulatory filings of rare disease products is preferred. Demonstrated excellence in developing, mentoring, and managing staff. Proven leadership and ability to positively influence colleagues and key decision-makers. Demonstrated collaboration skills working cross-functionally, maintaining strong stakeholder relationships, influencing direction, voicing opinion, and communicating. Benefits & Additional Information Compensation range: $145,000-$230,000 annually plus additional bonus, benefits and relocation support If you are interested please apply to be considered.

US$145000 - US$230000 per year + bonus, relocation support
Los Angeles
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Scientist, Analytical Development

We are seeking a highly skilled and motivated Analytical Scientist to join our team. The ideal candidate will be a SME in method development with extensive experience in injectable dosage forms. This role requires a Ph.D. in a relevant field and at least 2 years of experience working with Small Molecules. Key Responsibilities: Develop and validate analytical methods for injectable dosage forms. Conduct routine and non-routine analysis of pharmaceutical products using advanced analytical techniques. Collaborate with cross-functional teams to support product development and ensure compliance with regulatory standards. Troubleshoot and optimize analytical methods to improve efficiency and accuracy. Prepare and review technical documents, including protocols, reports, and standard operating procedures (SOPs). Stay current with industry trends and advancements in analytical technologies. Qualifications: Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field. Minimum of 2 years of experience in small molecule analysis. Expertise in method development and validation for injectable dosage forms. Proficiency in using analytical instruments such as HPLC, GC, MS, and others. Strong problem-solving skills and attention to detail. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Preferred Qualifications: Experience with regulatory submissions and compliance. Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

US$100000 - US$120000 per year
New Jersey
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Scientist, Analytical Development

We are seeking a highly skilled and motivated Analytical Scientist. The ideal candidate will be a SME in method development with extensive experience in injectable dosage forms. This role requires a Ph.D. in a relevant field and at least 2 years of experience working with Small Molecules. Key Responsibilities: Develop and validate analytical methods for injectable dosage forms. Conduct routine and non-routine analysis of pharmaceutical products using advanced analytical techniques. Collaborate with cross-functional teams to support product development and ensure compliance with regulatory standards. Troubleshoot and optimize analytical methods to improve efficiency and accuracy. Prepare and review technical documents, including protocols, reports, and standard operating procedures (SOPs). Stay current with industry trends and advancements in analytical technologies. Qualifications: Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field. Minimum of 2 years of experience in small molecule analysis. Expertise in method development and validation for injectable dosage forms. Proficiency in using analytical instruments such as HPLC, GC, MS, and others. Strong problem-solving skills and attention to detail. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Preferred Qualifications: Experience with regulatory submissions and compliance. Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

US$100000 - US$120000 per year
New Jersey
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Analytical Scientist

We are seeking a highly skilled and motivated Analytical Scientist. The ideal candidate will be a SME in method development with extensive experience in injectable dosage forms. This role requires a Ph.D. in a relevant field and at least 2 years of experience working with Small Molecules. Key Responsibilities: Develop and validate analytical methods for injectable dosage forms. Conduct routine and non-routine analysis of pharmaceutical products using advanced analytical techniques. Collaborate with cross-functional teams to support product development and ensure compliance with regulatory standards. Troubleshoot and optimize analytical methods to improve efficiency and accuracy. Prepare and review technical documents, including protocols, reports, and standard operating procedures (SOPs). Stay current with industry trends and advancements in analytical technologies. Qualifications: Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field. Minimum of 2 years of experience in Small Molecule analysis. Expertise in method development and validation for injectable dosage forms. Proficiency in using analytical instruments such as HPLC, GC, MS, and others. Strong problem-solving skills and attention to detail. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Preferred Qualifications: Experience with regulatory submissions and compliance. Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

US$100000 - US$120000 per year
New Jersey
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Associate Scientist (Cell Based Assays)

Role Description This is a full-time, on-site position for a Cell-based Assay Scientist located in Towson, MD. The Cell-based Assay Scientist will be responsible for conducting daily cell-based assays, analyzing data, and collaborating with cross-functional teams to develop and optimize assays. Key responsibilities include: Performing routine cell-based assays Analyzing and interpreting experimental data Collaborating with cross-functional teams to develop and optimize assays Maintaining accurate and detailed records of experiments and results Ensuring compliance with laboratory safety protocols and procedures Qualifications Extensive experience in cell culture techniques and cell-based assays Proficiency in data analysis and interpretation Strong attention to detail and organizational skills Excellent written and oral communication skills Ability to work effectively in a team environment Bachelor's or Master's degree in Biology, Biochemistry, or a related field Preferred: 1-2 years of industry experience in a biotech, pharma, or CRO setting

Negotiable
Baltimore
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Associate Director, Process Management - Clinical R&D

We are seeking a dynamic and strategic Associate Director, Process Management to create and drive business process optimization and continuous improvement in support of the growth and organizational effectiveness of our Clinical Research & Development team. This role requires a minimum of 3 days a week of onsite presence in either our California or New Jersey offices. About You: The ideal candidate is a collaborative and dynamic individual with a strong background in developing and executing robust business processes to improve efficiency, optimize resources, and reduce errors and compliance risks. You have experience engaging and organizing subject matter experts and cross-functional groups to identify gaps and inefficiencies and taking action to bridge these gaps through process optimization. Additionally, you have a strong background in the end-to-end clinical drug development process. Key Responsibilities: Lead project teams in creating, reviewing, and maintaining procedural documents (e.g., SOPs, policies, job aids), process maps, and personnel qualification strategies. Partner with Business Process Owners to ensure processes integrate with the end-to-end clinical drug development process, delivering efficiencies and mitigating compliance risks. Identify gaps and inefficiencies in current business processes and opportunities for improvement. Implement tools to collect and measure relevant data, identify key performance indicators (KPIs), and produce data-driven analyses of critical functions. Define and evaluate metrics to monitor the effectiveness of existing business processes. Collaborate with Business Process Owners and IT System Owners in the design, implementation, and release management of clinical systems (e.g., Clinical Trial Management System, electronic Trial Master File). Work with functional leaders, SMEs, and Clinical Quality Assurance to define compliance and business requirements, prioritizing core business processes based on strategic importance, regulatory requirements, and business impact. Develop and implement strategies to ensure ongoing inspection readiness for clinical trials. Support GCP audits and inspections by regulatory authorities and business partners. Develop and deliver training programs for new/updated operational procedures or clinical systems, including documentation, tools, and training to support adoption. Stay informed about changes in regulations, industry standards, and best practices. Qualifications: 10+ years of clinical drug development experience with a Bachelor's degree or 8+ years with a postgraduate degree. Experience in the biotechnology or pharmaceutical industry is required. In-depth knowledge of ICH-GCP, EMEA guidelines, and other relevant regulations and guidelines. Demonstrated ability to lead and influence change in process development and system implementation. Ability to collaborate effectively with cross-functional teams and subject matter experts. Proven ability to synthesize information from multiple sources and make risk-based decisions. Experience with Veeva Quality Vault and Veeva Clinical Platform is preferred. Excellent written, organizational, and interpersonal skills. Ability to work onsite at least 3 days a week. Compensation and Benefits: At Biopharmaceutical Company, employee compensation includes bonus and equity compensation, along with several generous benefit programs, including: 401k plan with company matching Medical (premiums covered by Biopharma company at 95%), dental, and vision insurance (premiums covered by Biopharma company at 100%) Mental health and wellness benefits Weeklong summer and winter holiday shutdowns Generous paid time off and holiday policies Life/AD&D Insurance (premiums covered by Biopharma company at 100%) and optional supplemental employee-paid life/AD&D policies Enhanced parental leave benefit Daily subsidized lunch program when on-site Join Biopharma company and be part of a team dedicated to advancing clinical research and development through innovative process management!

US$122000 - US$190000 per year
Hayward
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Head of CMC

Summary: This Biotech seeking a dynamic and experienced Head of CMC with a strong track record of developing small molecule programs. This pivotal role will oversee the development and implementation of CMC strategies to ensure the successful progression of our therapeutic candidates from discovery through clinical development and commercialization. Key Responsibilities: Develop and execute CMC strategies for drug development programs. Oversee all aspects of drug substance and drug product manufacturing. Ensure compliance with regulatory requirements and industry standards. Manage relationships with external partners, including CMOs and CROs. Lead and mentor a team of CMC professionals. Collaborate with cross-functional teams to support project timelines and objectives. Qualifications: Ph.D. in Chemistry, Chemical Engineering, or a related field. Minimum of 12 years of experience in CMC roles within the biotech or pharmaceutical industry. Proven track record of successful IND/IMPD/NDA submissions and regulatory interactions. Strong leadership and team management skills. Excellent communication and interpersonal abilities.

US$250000 - US$300000 per year
Cambridge Springs
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Scientist III Formulation Biologics

Summary: This growing Biotech is looking for a strong drug product development scientist to join their CMC team. This role involves formulation development, analytical testing, drug product manufacturing, and support for pre-clinical and clinical studies. The ideal candidate should be highly motivated, able to multitask, and thrive in a dynamic environment. Responsibilities: Lead formulation development and drug product manufacturing activities. Act as an SME in developing stable formulations for clinical-stage biotherapeutics. Design and evaluate formulations through stability studies. Perform analytical testing to assess product stability. Oversee DP container selection and Fill/Finish processes with CDMOs. Ensure GMP compliance during manufacturing. Lead compatibility studies of clinical administration components. Collaborate with internal teams and external partners. Contribute to regulatory filings and technical reports. Manage day-to-day lab activities and maintain equipment. Engage in scientific discussions and present findings. Qualifications: MS/PhD in Biochemistry, Biophysics, Chemical Engineering, or related field. Minimum of 8 years of biotech industry experience in formulation development and GMP DP Fill/Finish manufacturing. Expertise in formulation development methodologies and analytical techniques for mAbs, ADC's, Bispecifics, or fusion proteins is highly desired. Strong understanding of cGMP regulations. Excellent communication and multitasking skills.

US$100000 - US$130000 per year
Maryland
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Associate Director/Director, CMC

Associate Director / Director - CMC (Chemistry, Manufacturing, and Controls) Location: Brisbane, CA Department: R&D Employment Type: Full-Time, On-site OPPORTUNITY We are seeking an Associate Director / Director, CMC to be a key player in our product development teams, providing support across all developmental and clinical programs. The successful candidate will manage a network of CDMOs for Drug Substance and Drug Product manufacturing for our pipeline. KEY RESPONSIBILITIES Associate Director Level: Design, develop, and validate analytical methodologies for our pipeline. Identify opportunities to improve productivity and efficiency in projects and analytical science. Collaborate with diverse teams, including CDMO analytical science teams. Lead analytical science in project teams, ensuring alignment and fostering productive relationships with other core functions. Ensure data integrity and promote knowledge sharing throughout the medicine development lifecycle. Ensure compliance with regulatory standards including GMP, ICH, EMA, and FDA guidelines. Support the preparation of global regulatory submissions, scientific reports, and patents. Develop phase-appropriate quality control strategies for drug substance and drug product. Manage drug substance and drug product stability study programs. Develop scientifically sound and data-driven specifications. Oversee analytical and QC activities at CDMOs and Contract Testing Laboratories, including the review and approval of test records, forms, methods, protocols, and reports. Identify and develop suitable analytical methods for comprehensive characterization of drug substances, drug products, associated impurities, and excipients. Maintain documentation within the quality management system. Experience with various cultures, as CDMOs are global, with potential for global travel. Director Level: Provide broad CMC support for internal programs from GLP tox through IND clinical programs. Ensure timely Drug Substance/Drug Product supply for non-clinical and clinical studies. Assist in the preparation and review of CMC sections of regulatory submissions, including IND, BLA, NDA, and MAA. Manage CMOs for process development and manufacturing of Drug Substances and Drug Products for toxicology and cGMP supplies. Develop and execute CMC strategies for early and late phase Drug Substance/Drug Product clinical supplies. Implement processes and controls for regulatory materials, intermediates, and drug substances and products. Coordinate with internal and external analytical/quality control, quality assurance, and regulatory team members to resolve technical issues or deviations during cGMP production. Create and manage contracts, requests for pricing, supply agreements, etc., related to drug substance and drug product manufacturing. Ensure activities align with established Quality Agreements. Author, review, and adjudicate relevant CMC sections for US and ex-US regulatory filings as needed. Work closely with cross-functional teams to ensure seamless transitions between drug substance and drug product programs and suppliers. Develop and maintain collaborative relationships with internal stakeholders (e.g., Discovery, Non-Clinical, CMC, Clinical Operations, Regulatory, Quality, Finance, etc.) to deliver on internal goals and objectives. REQUIRED QUALIFICATIONS Master's Degree in a relevant scientific discipline. Prior experience with CMC development in gene therapy is highly desired. Minimum of 10 years of experience in biotech for large and small molecules (Director); minimum of 8 years of experience (Associate Director). Strong process understanding in one or more of the following: biologics, oligonucleotide, cell therapy, viral vectors, gene therapy, or LNP. Experience in managing external CDMOs for DS/DP production. Strong understanding of phase-appropriate analytical development and manufacturing strategies for large and small molecules. Experience with US and EU CMC regulatory expectations, technical transfers, and complex development & manufacturing activities. Excellent people manager and cross-functional leader, able to lead diverse and complex teams with demonstrated success. Ability to travel both domestically and internationally, as needed. PREFERRED QUALIFICATIONS Previous experience with CMC development in gene therapy. Previous experience managing CDMOs for outsourced manufacturing. Extensive understanding of cGMP regulations. Previous experience working in small to midsize biotech. Previous experience in CMC development of gene therapy products. Previous experience in small molecule and biologics manufacturing. Previous experience in formulation development for complex products like lipid nanoparticles. Experience with various cultures, as CDMOs are global, with potential for global travel. BENEFITS Company-paid health/vision/dental benefits. Unlimited vacation and generous sick time. Company-sponsored meals and snacks. Wellness, caregiver, and ergonomics benefits. 401(k) with company matching. Base Salary Range: $170,000 - $215,000 Actual base salary will be determined by relevant professional experience, applicable skills, and internal equity. Would you like any further modifications or additional details?

US$170000 - US$215000 per year
San Francisco
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Clinical Scientist

Title: Clinical Scientist (Contract Position) Introduction: A renowned biotechnology firm based in Redwood City, United States is seeking an experienced and dedicated Clinical Scientist. This contract position offers a challenging yet rewarding opportunity to contribute significantly within the immunology space while managing clinical sites efficiently. Key Responsibilities: -Collaborate with the physician lead to plan and oversee clinical studies focusing on mast cell and stem cell diseases, providing support for medical monitoring activities. -Gather, analyze, interpret, and review clinical data from assigned studies. -Support clinical data review and cleaning processes for key studies in the urticaria and stem cell programs, including generating and resolving queries. -Engage directly with study sites to facilitate effective communication and exchange of information. -Prepare study reports, presentations, and publications to share findings with internal and external stakeholders. -Actively participate in weekly study execution, clinical study team, and data review meetings. -Partner with cross-functional teams, including clinical operations, medical affairs, regulatory affairs, and biostatistics, to ensure the successful execution of assigned programs. Requirements: Education and Experience Advanced degree (MD, PharmD, PhD, or equivalent) in a relevant scientific or medical field required. 0-3 years of pharmaceutical industry experience, preferably in immunology. Strong understanding of clinical trial design, methodology, and regulatory standards (e.g., GCP, ICH). Proficient in data analysis, interpretation, and statistical methods. Excellent written and verbal communication skills for diverse audiences. Experience in hematological malignancies, transplant studies, immunological, or dermatological research is a plus. Title commensurate with experience. Skills and Competencies Strong project management, organizational, and analytical skills. Exceptional problem-solving and communication abilities. Ability to collaborate effectively in a matrixed environment. Proficiency in statistics, data interpretation, and relevant tools. Bay Area location preferred. Experience with electronic data capture systems is a plus. Apply now if meeting these criteria aligns with where you envision taking your expertise next!

Negotiable
Redwood City
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R&D News & Insights

Life Sciences Salary Guides of 2023 Image
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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How to Stand Out to Top R&D Talent as an Employer  Image
r-and-d

How to Stand Out to Top R&D Talent as an Employer

Discover insights from Principal Consultant Ed Curry ahead of the American Society of Gene & Cell Therapy (ASGCT) annual meeting in May 2023. With a particular passion for drug discovery and pre-clinical, Ed works with top life sciences employers and successfully builds and manages their R&D talent pipelines. In this interview, Ed shares his thoughts on how employers can stand out to R&D talent and give themselves the best chance at attracting top talent. Ed will be covering topics such as how employers can create a compelling offer, streamline their hiring process, and how to differentiate yourself from competitors. What is the talent market like right now in R&D?Talent remains a top challenge for those hiring. A recent C-suite survey by Deloitte noted that bringing on and retaining talent is a top priority for business leaders, and even more narrowly in the MedTech space, there is a focus in recruiting in the R&D market. The market is still very hot, but macroeconomic conditions have had an impact of course when it comes to hiring. We have seen some companies reduce headcount or even close their doors through sometimes no fault of their own, in part because of such high interest rates. To an extent it could give the illusion that the candidate pool is larger and that they have more options, but it actually isn’t that clear-cut. For example, with a recent role we saw 80 applicants, but only four of them actually had the required skillset. Top talent is therefore always in demand, but it is also always harder to find. These conditions can also result in top talent becoming even more passive to new opportunities, due to the uncertainty. Unfortunately, we have recently seen great companies making layoffs, and some candidates can be concerned about being the last one in. These people are who would fill those business-critical roles, so it is up to us as a leading talent partner to source from a tight talent pool and work with a candidate to enable that move, even in more precarious economic times. Finding the right people as market specialists is what we do best.How can organizations win over the most sought-after talent in a highly competitive space? Macro events are playing on people’s minds, and as a result of this great science is not the only selling point when obtaining talent. Promising biotechs have had to lay off great scientists for example, demonstrating that not every project can be pursued. Informing candidates about an exciting project is not enough anymore, instead companies recruiting need to outline short, medium, and long-term plans. They also need to talk about what funding they have, because top professionals may be incentivized to move to somewhere they perceive as more stable. Just like a relationship is 50/50, an interview should be the same. We recommend that clients should sell themselves and the company as much as they expect the candidate to sell. Strong professionals are going to be interviewing elsewhere, so consider that they are also interviewing you. Also, remember to do this from the very start, and not just at the end of the process. From the very first interview, hiring managers, HR, and talent acquisition are being equally interviewed by talent. Another aspect for organizations to consider highlighting is the growth opportunities you offer, and how you set up people for success. Alongside career advancement and skill development, professionals still put a premium on a good work/life balance, with company culture also playing a part here. What talent strategies would you recommend to hiring managers to differentiate themselves from other players in winning talent?My number one recommendation is to streamline candidate onboarding. Lack of speed results in candidates going elsewhere and interview fatigue is a real problem, so set yourself apart with being quick. Instead of three interviews, get all three people into one and cut down stages, because when top talent is scarce, they will be looking at other opportunities. Another strategy to implement is aligning your selling points to the individual interviewing where possible. This means getting to know the person interviewing really well to understand their own unique motivations, as well as working with a talent partner who has that information. For example, I recently worked with a single parent and placed them into an organization that could accommodate the flexible working policy they desired. Also assume that good candidates will be getting multiple offers, so don’t put people on the backburner. Give feedback where possible, because communication is super important. We’ve seen a client not progress with an individual, but because they gave comprehensive feedback, and I fed this back as well, it led to that person actually recommending a colleague of theirs for the role, who was actually placed. Reputation is critical, as both a company and a hiring manager. Where (if any) can organizations look for transferable skills to fill talent gaps?‘Purple unicorns’ do exist, but as their name suggests, they are hard to find. Sometimes a job description will describe something that isn’t possible, so I find it is very important during the intake call to differentiate between what is a nice to have, versus a must-have. Let’s take a neuromuscular R&D role where the client is working on Huntington’s and Parkinson’s projects. If a candidate has worked in the past on muscular dystrophy, is that okay for the client? That candidate might not know the particular disease inside out right now, but they can apply a similar knowledge and skillset to another disease. Here is where clients can make concessions, and also attract different talent. Consider looking towards adjacent industries, such as tech talent migrating into life sciences. As more and more biotechs develop a tech-focused footprint, there are only going to be so many life sciences professionals to go around, so maybe tech talent is where the industry can look for individuals who have a passion to make a difference in life sciences. How can tackling bigger, societal issues such as ED&I and ESG assist with talent attraction and retention? This is one of the reasons I love working in life sciences because I am fortunate to work with mission-driven individuals. The industry is one of the best places to tackle wider societal issues, it is a diverse sector that tackles these challenges head-on. I have noticed younger talent seems to think aligning values is very important, and that trend will only continue. Life sciences as an industry is addressing bias in clinical trials as historically there may have been some selection discrimination. The industry is also looking at how it can tackle climate change, for example one organization is exploring how it can genetically modify cows to decrease methane production.How do you see this market developing over the next 12 months?We saw just a few years ago clients throwing everything at candidates to get them in the door. This resulted in compensation, as well as title inflation. With the new macroeconomic environment, funding is tighter, and therefore being able to offer such compensation now may be a little trickier. The industry is now reverting back to normality after Covid-19 resulted in a lot of investment being funneled into it. The cost of living is also increasing, and this may mean that academic professionals may move from educational institutions to more lucrative roles. Last year was historically low for mergers and acquisitions in life sciences as well, but we do expect that to pick up. It will be interesting to see if cutting-edge, start-up biotechs partner with big pharmaceuticals, which provides an interesting science angle to candidates, with the funding backing and runways of a big player. As mentioned earlier, the tech industry has experienced change and we have seen more appetite for tech talent. DNA sequencing and automation in labs for example, as well as data processing, requires tech talent, so I believe we will continue to see movements from Big Tech to biotech. Organizations are spending billions on technology to advance their programs and products, so it’s important to mention machine learning and AI professionals as in-demand talent for the next 12 months and onwards. Finally, I firmly believe that venture capital will also invest in healthcare at large. Healthcare accounts for one-fifth of US GDP, so financial experts know it is a worthwhile investment. Therefore, while macroeconomic conditions have been a little pessimistic recently, 2023 and the year ahead is going to be great, and I can’t wait to see how it unfolds. Meet Ed at the American Society of Gene & Cell Therapy (ASGCT) annual meeting, or get in touch using the form below to discuss your hiring needs. ​ Edward Curry Principal Consultant​Request a call back from Ed

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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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How to Determine if a New Hire Will Fit into Your Company's Culture Image
Management & Culture

How to Determine if a New Hire Will Fit into Your Company's Culture

There’s no question that a company’s culture and ethos can help its employees feel more satisfied at work, increase employee retention and ultimately serve as a catalyst for its success. Company culture is seen as very important by professionals: survey data collected by Glassdoor shows that more than three quarters of professionals take the culture into account before applying for a job, and 56% say that they see the culture of a company as playing a more significant role than salary in determining overall job satisfaction. Given the role that it plays, cultural fit should be a key priority for employers.Why is cultural fit important?If somebody is a good cultural fit for a company, they are far more likely to be an engaged, motivated employee who derives satisfaction from their role. There is a greater chance that they will see the job as more than just a source of income and as such, they will be more likely to go above and beyond in the workplace and may even inspire others to follow in their footsteps.Hiring for cultural fit therefore makes good business sense. 10-25% of new employees decide to leave within six months of starting work, and one reason that professionals give for quitting is that they feel that they are a poor fit for the company culture. Choosing people for the job who are a natural fit for the company’s values and working practices is a great way to avoid these problems from arising.How to hire for cultural fit?Given the importance of company culture, businesses are increasingly hiring for cultural fit. This involves defining what your culture is all about and incorporating questions at interview stage that relate to your interviewees’ values, motivations and aspirations.Define your company’s cultureThe first step is to describe your company’s culture in writing. What are the values, beliefs and ethics that characterize your company’s operations and working environment? If you are struggling to capture the essence of your culture, it might be worth asking current employees about how they feel about the company and its working practices. It is recommended that you use such feedback when writing or updating a mission statement and articulating your company values. Include these on your website and on all your digital platforms, in addition to testimonials from your current employees.Demonstrate your values throughout the interview processAsking values-based interview questions is one of the best ways to identify candidates who share your values and will be a good fit in the workplace.You should also draw attention to the benefits that you offer your employees. 56% of CFOs in the Asia-Pacific (APAC) have said that they are considering expanding benefits, including flexible working arrangements (FWAs), in a bid to retain their top talent. If you offer flexible working roles, ensure that your staff relay this information at interview stage.Cover the right questionsIf you’re wondering how to determine if a candidate is a good fit, asking the following questions will help shed light on the personality of your interviewees and their alignment with your values:What motivates you? How do you handle conflict in the workplace?What work environment supports innovation and productivity levels? Give me an example of something that you have taught yourself in the last six monthsWhat experiences have shaped your outlook on life?What are you most proud of?Utilize personality testsPersonality tests provide valuable insights into how prospective employees approach problems. They can also shed light on their ability to work alongside others and offer further information about their interests and preferences.Some of the most common personality tests used by employers include the Myers-Briggs Type Indicator, the Caliper Profile and the 16 Personality Factor Questionnaire.Other key considerationsWhilst cultural fit is of great importance, it should be weighed alongside other factors. Hiring solely for cultural fit can perpetuate bias and lead to a lack of diversity within the workplace as a result. It’s also important to take into consideration an applicant’s qualifications, work experience, career aspirations and skill set when assessing their suitability for a role in your organization.Secure Life Sciences Talent with EPM ScientificAre you looking to solve your talent challenges? EPM Scientific offers bespoke talent solutions across Life Sciences A combination of our specialist account management service, ongoing support and reporting, and hiring advice allows us to find you exactly the people you need, when you need them. Register your vacancy or request a call back today.Our Talent Expertise​​​

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The Benefits of using Life Sciences contractors/freelancers Image
commercial

The Benefits of using Life Sciences contractors/freelancers

The use of life sciences contractors and freelancers is becoming increasingly popular, and for good reason. Not only are they able to provide specialized expertise, but they also offer a wide range of benefits that can help a business grow and thrive. Here are 10 of the top benefits of using life sciences contractors and freelancers.1. Cost Savings: Hiring contractors and freelancers is often significantly cheaper than hiring full-time staff. This is because you only pay for the services you need, when you need them.2. Flexibility: Contractors and freelancers offer flexibility that traditional employees cannot. You can easily scale up or down your workforce as needed, allowing you to meet fluctuating demands.3. Access To Specialized Expertise: Life sciences contractors and freelancers often have specialized skills and expertise that can be invaluable to a business.4. Faster Turnaround Time: When you need something done quickly, hiring a contractor or freelancer is often the fastest way to get the job done.5. Reduced Overhead: Contractors and freelancers don’t require the investment in overhead expenses that full-time employees do, such as office space and benefits.6. Fresh Perspective: Bringing in a contractor or freelancer can bring a fresh perspective to a project and help generate new ideas.7. Lower Risk: Hiring a contractor or freelancer reduces the risk that comes with hiring full-time employees. If a project doesn’t meet expectations, you can simply end the contract and look for a better fit.8. Increased Productivity: With more specialized expertise, contractors and freelancers can often complete projects more efficiently and quickly than full-time employees.9. Focus On Core Activities: By outsourcing more specialized tasks to contractors and freelancers, businesses can focus more on their core activities and reduce distractions.10. Improved Morale: Hiring contractors and freelancers can help to improve morale among existing staff, as they don’t have to take on extra tasks they may not be qualified or comfortable with.At EPM Scientific, we are the leading provider of life sciences contract and freelance recruitment services. We understand the importance of finding the right talent for the job, and have the experience and expertise to help you find the perfect candidate for your business. Request a call back from us todayto learn more about how we can help you find the perfect contractor or freelancer for your business.

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