Senior Biostatistician

Xenon Pharmaceuticals Inc.

. Provide statistical support for assigned clinical development programs or trials .

Posted 9/15/2026full-timeBoston • Massachusetts • United StatesSenior💰 $155,000 - $173,200 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Expertise in statistical methodologies and programming, particularly in SAS, with a strong focus on clinical trial design and regulatory compliance. Proven ability to collaborate across functional areas and manage CRO deliverables while adhering to industry standards.

Highest-signal resume keywords

Ph.D. In Statistics Or BiostatisticsSAS Programming LanguageStatistical Analysis PlansFDA Regulations KnowledgeCRO Management Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical MethodologiesClinical Trial DesignStatistical ModelingStatistical AnalysisCDISC StandardsADaM RequirementsR Programming LanguageData ManagementStatistical ReviewNDA/MAA Submission

Soft Skills

Strong Communication SkillsOrganizational SkillsTime Management SkillsInterpersonal SkillsAbility To Build Credibility

Industry Keywords

Pharmaceutical IndustryBiotech IndustryCNS ExperienceICH GuidelinesCompany PoliciesCode Of Business Conduct And Ethics

About the role

Key responsibilities & impact

Provide statistical support for assigned clinical development programs or trials
Participate in the development of study protocols
Develop statistical analysis plans and analysis specifications for programming implementation of statistical analyses
Provide statistical input into data management and programming deliverables, including data collection tools and analysis datasets
Develop statistical programs for ad-hoc requests, manuscripts, and presentations
Provide statistical review of scientific reports and publications
Collaborate with other functional areas on project deliverables and timelines
Provide oversight of CRO deliverables to ensure quality and accuracy
Adhere to company and department SOPs and working practices
Act in accordance with Company policies, including the Code of Business Conduct and Ethics
Perform other duties as assigned
Report to the Director, Biostatistics

Requirements

What you’ll need

PH.D. in Statistics or Biostatistics with a minimum of 2 years of statistical experience in the pharmaceutical or biotech industry, or Master with a minimum of 5 years of statistical experience
Up-to-date knowledge of statistical methodologies related to areas such as clinical trial design, statistical modeling and analysis
Knowledge of applicable FDA regulations and ICH guidelines
Advanced knowledge of the SAS programming language; knowledge of R or similar language a plus
Knowledge of CDISC standards, including ADaM requirements
Experience in CNS preferred
Experience in CRO management preferred
Experience in NDA/MAA submission a plus
Strong organizational and time management skills, and the ability to prioritize multiple deliverables and ad-hoc requests
Strong communication skills, both oral and written
Strong interpersonal skills, ability to build credibility and trust inside and outside the Company
Ability to travel up to 10%, both domestically and internationally

Benefits

Comp & perks

Target bonus
Stock options
Medical insurance
Dental insurance
Vision insurance
Short-term disability insurance
Long-term disability insurance
Accidental death & dismemberment insurance
Life insurance programs
Employee Assistance Program
Travel insurance
Retirement savings programs with company matching contributions
Vacation
Personal days
Sick days
End-of-year company shutdown
Training, Learning & Development program
Tuition Assistance program for advanced degrees