What Youβll Do:
- 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
Who You Are:
- Enjoy designing and interpreting observational studies and work collaboratively with different functions.
Required Skills:
- 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:
- Medical, Dental, Vision & Life insurances
- Fitness & Wellness programs including fitness reimbursement
- Short- and Long-Term Disability insurance
- Minimum of 15 days paid vacation; end-of-year shutdown (Dec 26βDec 31)
- Up to 12 paid holidays + 3 paid days off for Personal Significance
- 80 hours sick time per calendar year
- Paid Maternity and Parental Leave
- 401(k) with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement up to $10,000 per calendar year
- Employee Resource Groups participation