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Xenon Pharmaceuticals Inc.

Clinical Scientist 2, Clinical Development

Xenon Pharmaceuticals Inc.

Clinical Scientist contributing to clinical development activities in a biopharmaceutical company focused on neuroscience. Engaging in study planning, execution, and regulatory strategy alignment.

Posted 6/10/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesMid-LevelSenior💰 $108,500 - $152,600 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, and clinical development planning
  • Support the development, implementation, conduct, oversight, and reporting of clinical trials
  • Perform comprehensive literature reviews and maintain current knowledge of relevant disease areas
  • Participate in the review and interpretation of clinical data
  • Collaborate cross-functionally with Clinical Operations, Data Management, etc.
  • Draft and contribute to clinical and regulatory documents
  • Support or lead scientific interactions with CROs, investigators, and external collaborators
  • Develop and maintain productive relationships with external scientific experts

Requirements

What you’ll need
  • MSc or PhD degree in Life Sciences, Biomedical Sciences, Pharmacology or related scientific discipline
  • 2-5 years of post-doctoral experience and/or relevant industry experience, preferably in neurosciences
  • Experience in clinical research and clinical development with strong understanding of study design and clinical data review
  • Experience drafting, reviewing, or supporting clinical and regulatory documentation
  • Working knowledge of GCP, ICH guidelines, and familiarity with FDA and EMA environments
  • Strong written, verbal, interpersonal, and presentation skills
  • Strong organizational skills and attention to detail
  • Experience in neuroscience, CNS, psychiatry, neurology, or related therapeutic areas is preferred
  • Experience working with investigators, CROs, vendors, and external scientific experts is preferred.

Benefits

Comp & perks
  • Health insurance
  • Retirement savings programs with company matching contributions
  • Employee Assistance Program
  • Travel insurance
  • Short-& long-term disability benefits
  • Accidental death & dismemberment benefits
  • Life insurance programs
  • Paid time off, including vacation, personal days, and sick days.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
study designprotocol developmentclinical development planningclinical trialsliterature reviewsclinical data reviewclinical documentationregulatory documentationGCPICH guidelines
Soft Skills
scientific leadershipinterpersonal skillsorganizational skillsattention to detailwritten communicationverbal communicationpresentation skills
Certifications
MScPhD