Associate Director, Pharmacovigilance Scientist

Biogen

Cambridge, MA, United States
Base: $172,000.00-$237,000.00; bonus/equity: cash ...
Hybrid
Pharmacovigilance signal management
Aggregate safety report authoring
Eu risk management plan expertise
As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will play a critical part in ensuring the safety and efficacy of our products while fostering a collaborative and high-performing team environment

Job Summary

  • As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will play a critical part in ensuring the safety and efficacy of our products while fostering a collaborative and high-performing team environment.
  • Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
  • At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve.

Matching Summary

As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will play a critical part in ensuring the safety and efficacy of our products while fostering a collaborative and high-performing team environment.

Salary

Base: $172,000.00-$237,000.00; Bonus/Equity: Cash bonus and equity incentives available; Benefits: Medical, Dental, Vision, Life insurance, wellness programs, paid time off, 401(k), stock purchase plan, tuition reimbursement

Skills & Requirements

Must-have

  • Pharmacovigilance signal management
  • Aggregate safety report authoring
  • EU Risk Management Plan expertise
  • Regulatory filing support
  • Team management and mentoring
  • Compliance with global PV regulations

Nice-to-have

  • Collaborative team environment
  • Strong organizational skills
  • Ability to distill complex data
  • Cross-functional communication
  • Adapt resource needs independently

Key Requirements

  • Minimum 10 years Pharmacovigilance experience
  • Experience in safety signal management
  • Experience authoring EU Marketing Authorization filings
  • Experience authoring Risk Management Plans and DSURs
  • Ability to interpret scientific and medical data

Work Rights

Not specified

Tailored Resume

Cover Letter