Associate Pharmacovigilance Scientist

Biogen

Cambridge, MA, United States
Base: $106,000.00-$138,000.00; bonus/equity: cash ...
Signal management activities
Aggregate report planning
Safety literature reviews
The Associate PV Scientist serves as a critical team member within the Safety Surveillance and Aggregate Report (SSA) team for products or product groups, including supporting with signal management activities, contributing to aggregate report planning / authoring, responding to ad hoc regulatory responses, and conducting safety literature reviews

Job Summary

  • The Associate PV Scientist serves as a critical team member within the Safety Surveillance and Aggregate Report (SSA) team for products or product groups, including supporting with signal management activities, contributing to aggregate report planning / authoring, responding to ad hoc regulatory responses, and conducting safety literature reviews.
  • With the ability to distill complex data into clear, actionable insights, you shine in a collaborative team setting.
  • Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

The Associate PV Scientist serves as a critical team member within the Safety Surveillance and Aggregate Report (SSA) team for products or product groups, including supporting with signal management activities, contributing to aggregate report planning / authoring, responding to ad hoc regulatory responses, and conducting safety literature reviews.

Salary

Base: $106,000.00-$138,000.00; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, & Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Paid Maternity and Parental Leave, 401(k) program, Employee stock purchase plan, Tuition reimbursement

Skills & Requirements

Must-have

  • Signal management activities
  • Aggregate report planning
  • Safety literature reviews
  • Clinical trial safety activities
  • Data review and verification

Nice-to-have

  • Distill complex data
  • Collaborative team setting
  • Fast-paced environment
  • Pioneering spirit
  • Inclusion and belonging

Key Requirements

  • Minimum 3 years industry experience
  • Minimum 3 years PV experience
  • Bachelor’s Degree in biologic or natural science; or health care discipline
  • Safety case processing experience preferable

Work Rights

Not specified

Tailored Resume

Cover Letter