Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Xenon Pharmaceuticals Inc.

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 & technologies
Google 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 resume
Applicant 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