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Clinical Scientist 3, Clinical Development
Xenon Pharmaceuticals Inc.Clinical Scientist 3 developing innovative therapeutics for neurological conditions at Xenon Pharmaceuticals. Leading clinical development activities and ensuring scientific rigor in execution.
Posted 6/10/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesMid-LevelSenior💰 $160,400 - $186,100 per yearWebsite
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Provide scientific leadership and independent contribution to study design, protocol development, endpoint strategy, and clinical development planning for assigned programs.
- Support the development, implementation, conduct, oversight, and reporting of clinical trials, ensuring scientific quality and alignment with program objectives.
- Perform comprehensive literature reviews and maintain current knowledge of disease areas, competitive landscape, emerging science, and regulatory developments relevant to assigned products and indications.
- Participate in the review, monitoring, summarization, and interpretation of safety, efficacy, pharmacokinetic, patient-reported outcome, and other clinical data to support development decisions and recommendations.
- Collaborate cross-functionally with Clinical Operations, Biometrics/Biostatistics, Data Management, Pharmacovigilance, Medical Writing, Regulatory, Translational Development, Medical Affairs, and other partners to support high-quality study execution and documentation.
- Draft, review, and contribute to clinical and regulatory documents, including study protocols, synopses, investigator brochures, clinical study reports, health authority submission content, briefing materials, abstracts, posters, and manuscripts.
- Support or lead scientific interactions with CROs, investigators, site personnel, and external collaborators to ensure consistency, scientific integrity, and effective study execution.
- Contribute to advisory boards, expert meetings, and other scientific interactions that support program development and evidence generation.
- Support the development of departmental processes, templates, standard operating procedures, and best practices as needed.
Requirements
What you’ll need- MSc or PhD degree in Life Sciences, Biomedical Sciences, Pharmacology or other professional doctorate in pharmaceutical sciences or a related scientific discipline
- At least 5-8 years of post-doctoral experience and/or relevant industry experience, preferably in neurosciences
- Experience in clinical research and clinical development with a strong understanding of study design, study conduct, clinical data review, and interpretation
- Experience drafting, reviewing, or supporting clinical and regulatory documentation and working effectively in cross-functional teams
- Working knowledge of GCP, ICH guidelines, and regulatory expectations, including familiarity with FDA and EMA environments
- Strong organizational skills, attention to detail, and the ability to work independently while contributing effectively in a team environment
- Experience in neuroscience, CNS, psychiatry, neurology, or related therapeutic areas is preferred
- Demonstrated ability to analyze complex scientific information, generate sound recommendations, and solve problems in a dynamic development environment
- Experience working with investigators, CROs, vendors, and external scientific experts is preferred
Benefits
Comp & perks- medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs
- Employee Assistance Program
- travel insurance
- retirement savings programs with company matching contributions
- vacation, personal days, sick days, and an end-of-year company shutdown
- expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchstudy designprotocol developmentclinical data reviewregulatory documentationpharmacokineticspatient-reported outcomesGCPICH guidelinesFDA
Soft Skills
scientific leadershiporganizational skillsattention to detailindependent workteam collaborationproblem-solvingcommunicationcross-functional collaborationscientific integrityadaptability
Certifications
MScPhD