Clinical Scientist
Job description
The Clinical Scientist is an individual contributor responsible for providing scientific expertise and leadership to Phase II–IV clinical development programs. This role contributes to study design, protocol development, and regulatory documentation, applying scientific judgment to interpret clinical data and literature in support of program strategy. The Clinical Scientist collaborates cross‑functionally to ensure scientific consistency, quality, and timeliness of clinical documents and supports internal and external scientific interactions that advance clinical programs.
Job requirements
Advanced degree in Life Sciences (PhD, PharmD, or MSc preferred; MD not required)Minimum of 2+ years of experience in clinical development, clinical research, or medical affairs with increasing responsibilityPrior experience supporting Phase II–III clinical trials (Phase IV experience a plus)Demonstrated ability to independently draft and review scientific and clinical documentsStrong understanding of GCP, clinical trial methodology, and regulatory expectationsExcellent scientific writing, data interpretation, and presentation skillsHighly organized, detail‑oriented, and able to manage multiple deliverables in a fast‑paced environment
Job responsibilities
Clinical & Scientific ContributionsContribute scientific input to the design and execution of Phase II–IV clinical trials, including study rationale, objectives, endpoints, and protocol contentServe as the scientific owner or primary contributor for assigned studies or components of a clinicalprogramInterpret clinical data and scientific literature to inform protocol development, program strategy, and internal decision‑makingIdentify scientific risks, data gaps, or inconsistencies and propose evidence‑based solutionsClinical Documentation & Regulatory SupportDraft, review, and maintain clinical trial protocols, study synopses, and related clinical documentsSupport preparation of clinical sections of regulatory submissions, briefing packages, and responsesEnsure scientific accuracy, clarity, and consistency across protocols, regulatory documents, and presentationsDevelop scientific narratives, data summaries, and slide content for governance, leadership, and board‑level discussionsCross‑Functional CollaborationAct as a scientific liaison with Clinical Operations, Biostatistics, Regulatory Affairs, Medical Affairs, and other cross‑functional partnersFacilitate cross‑functional discussions to resolve scientific questions and align on clinical strategy and timelinesTranslate complex scientific concepts into clear, concise messaging for non‑scientific stakeholdersExternal Scientific EngagementSupport scientific content for interactions with regulatory agencies, advisory boards, and Key Opinion Leaders (KOLs)Prepare scientific briefing materials and background documentation for external meetingsIncorporate feedback from external experts into clinical documentation and program strategy
Job benefits
Medical, Dental, Vision InsuranceLife/AD&DShort- and Long-Term Disability401(K) with large company matchHealth Saving Account (HSA) and Flexible Spending Account (FSA) with company matchWellness ProgramEmployee Assistance Program (EAP)Generous Paid Time Off (PTO)Disclaimer: The included statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
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The Clinical Scientist is an individual contributor responsible for providing scientific expertise and leadership to Phase II–IV clinical development programs. This role contributes to study design, protocol development, and regulatory documentation, applying scientific judgment to interpret clinical data and literature in support of program strategy. The Clinical Scientist collaborates cross‑functionally to ensure scientific consistency, quality, and timeliness of clinical documents and supports internal and external scientific interactions that advance clinical programs.
Job requirements
Advanced degree in Life Sciences (PhD, PharmD, or MSc preferred; MD not required)Minimum of 2+ years of experience in clinical development, clinical research, or medical affairs with increasing responsibilityPrior experience supporting Phase II–III clinical trials (Phase IV experience a plus)Demonstrated ability to independently draft and review scientific and clinical documentsStrong understanding of GCP, clinical trial methodology, and regulatory expectationsExcellent scientific writing, data interpretation, and presentation skillsHighly organized, detail‑oriented, and able to manage multiple deliverables in a fast‑paced environment
Job responsibilities
Clinical & Scientific ContributionsContribute scientific input to the design and execution of Phase II–IV clinical trials, including study rationale, objectives, endpoints, and protocol contentServe as the scientific owner or primary contributor for assigned studies or components of a clinicalprogramInterpret clinical data and scientific literature to inform protocol development, program strategy, and internal decision‑makingIdentify scientific risks, data gaps, or inconsistencies and propose evidence‑based solutionsClinical Documentation & Regulatory SupportDraft, review, and maintain clinical trial protocols, study synopses, and related clinical documentsSupport preparation of clinical sections of regulatory submissions, briefing packages, and responsesEnsure scientific accuracy, clarity, and consistency across protocols, regulatory documents, and presentationsDevelop scientific narratives, data summaries, and slide content for governance, leadership, and board‑level discussionsCross‑Functional CollaborationAct as a scientific liaison with Clinical Operations, Biostatistics, Regulatory Affairs, Medical Affairs, and other cross‑functional partnersFacilitate cross‑functional discussions to resolve scientific questions and align on clinical strategy and timelinesTranslate complex scientific concepts into clear, concise messaging for non‑scientific stakeholdersExternal Scientific EngagementSupport scientific content for interactions with regulatory agencies, advisory boards, and Key Opinion Leaders (KOLs)Prepare scientific briefing materials and background documentation for external meetingsIncorporate feedback from external experts into clinical documentation and program strategy
Job benefits
Medical, Dental, Vision InsuranceLife/AD&DShort- and Long-Term Disability401(K) with large company matchHealth Saving Account (HSA) and Flexible Spending Account (FSA) with company matchWellness ProgramEmployee Assistance Program (EAP)Generous Paid Time Off (PTO)Disclaimer: The included statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Apply Now