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Biogen

Associate Director, Epidemiology

Biogen

Associate Director, Epidemiology leading observational and post-market safety research at Biogen, a biotechnology company. Providing epidemiologic evidence and regulatory support across drug development programs.

Posted 8/25/2026full-timeCambridge • Massachusetts • 🇺🇸 United StatesSenior💰 $158,000 - $242,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in observational research methodologies, including cohort and database studies, while effectively collaborating across multi-disciplinary teams to generate evidence for regulatory compliance and decision-making.

Highest-signal resume keywords
PhD Or ScD In EpidemiologyEpidemiological Literature ReviewDatabase Study Design And InterpretationCohort Study Design And ExecutionRegulatory Activities In Pharmacovigilance

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Epidemiological Literature ReviewDatabase Study DesignCohort Study DesignDisease Incidence EstimationDisease Prevalence EstimationRisk Factor AnalysisEvidence Generation PlanningRegulatory CompliancePharmacovigilanceRisk Management Plans
Soft Skills
Team CollaborationDecision-Making
Certifications & Qualifications
PhD Or ScD In Epidemiology
Industry Keywords
PharmaceuticalBiotechnologyContract Research OrganizationPost-Market Safety StudiesObservational ResearchCohort StudiesRegistry-Based Studies

About the role

Key responsibilities & impact
  • Lead observational research including cohort, registry-based and database studies for disease understanding or post-market safety studies
  • Review and synthesize epidemiological literature
  • Provide estimates of disease incidence and prevalence, disease progression and disease-specific risk factors
  • Contribute to regulatory activities including periodic safety update reports, pharmacovigilance, and risk management plans
  • Collaborate cross-functionally for evidence generation planning and execution
  • Interact directly with research, development and post-market program teams
  • Provide concrete deliverables to support decision making, progress programs through development, and meet regulatory requirements

Requirements

What you’ll need
  • PhD or ScD in Epidemiology
  • At least 2 years experience in a pharmaceutical, biotechnology, or contract research organization setting
  • Expertise in literature review and synthesis
  • Expertise in designing, conducting and interpreting large database studies and cohort studies
  • Ability to work in a multi-disciplinary team setting and use a team approach to decision-making

Benefits

Comp & perks
  • Short-term and long-term incentives, including cash bonus and equity incentive opportunities
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • Minimum of 15 days of paid vacation
  • Additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays
  • 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation