Associate Medical Director, Global Drug Safety

Biogen

Cambridge, MA, United States
Base: $194,000.00-$267,000.00; bonus/equity: cash ...
Global pharmacovigilance for products
Safety data review and analysis
Clinical trial design involvement
As the Associate Medical Director, Global Drug Safety, you will play a pivotal role in safeguarding patient well-being and shaping the safety strategy for investigational and marketed products

Job Summary

  • As the Associate Medical Director, Global Drug Safety, you will play a pivotal role in safeguarding patient well-being and shaping the safety strategy for investigational and marketed products.
  • 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 future potential.
  • Biogen offers a full and highly competitive range of benefits designed to support employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

As the Associate Medical Director, Global Drug Safety, you will play a pivotal role in safeguarding patient well-being and shaping the safety strategy for investigational and marketed products.

Salary

Base: $194,000.00-$267,000.00; Bonus/Equity: Cash bonus and equity incentives available; Benefits: Medical, Dental, Vision, Life insurance, wellness programs, paid time off, 401(k) with company match, stock purchase plan, tuition reimbursement

Skills & Requirements

Must-have

  • Global pharmacovigilance for products
  • Safety data review and analysis
  • Clinical trial design involvement
  • Benefit-risk profile management
  • Leadership of high performing teams
  • Knowledge of US and EU regulations

Nice-to-have

  • Mentoring and guidance skills
  • Commitment to inclusion and belonging
  • Experience in both academic and industry settings
  • Pioneering spirit and commitment to excellence

Key Requirements

  • MD or MD/PhD required
  • Minimum 3+ years pharmaceutical industry or clinical care experience
  • Experience specific to pharmacovigilance
  • Prior clinical trials experience preferred
  • Knowledge of pre- and post-marketing US and EU regulations

Work Rights

Not specified

Tailored Resume

Cover Letter