Senior Scientific Director, Serm

GSK

Cambridge, MA, US
Base: $217,800 to $363,000 (us locations); bonus/e...
Not specified (assumed hybrid based on location options)
Pharmacovigilance and risk management
Safety evaluation and signal detection
Cross-functional matrix team leadership
GSK is seeking a Senior Scientific Director in Pharmacovigilance to lead safety evaluation and risk management for their global assets, particularly within oncology. The ideal candidate will have over 10 years of experience in the pharmaceutical or biotech industry, particularly in drug safety, and possess strong leadership and communication skills

Job Summary

  • GSK aims to positively impact the health of 2.5 billion people by the end of the decade through innovative vaccines and medicines.
  • The role leads pharmacovigilance and risk management planning, safety governance, and cross-functional teams to ensure patient safety globally.
  • The position offers a competitive salary range, annual bonus, long term incentives, and comprehensive benefits including healthcare and paid leave.

Matching Summary

Match Score: 85

GSK is seeking a Senior Scientific Director in Pharmacovigilance to lead safety evaluation and risk management for their global assets, particularly within oncology. The ideal candidate will have over 10 years of experience in the pharmaceutical or biotech industry, particularly in drug safety, and possess strong leadership and communication skills.

Salary

Base: $217,800 to $363,000 (US locations); Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, retirement, paid holidays, vacation, caregiver/parental and medical leave

Skills & Requirements

Must-have

  • Pharmacovigilance and risk management
  • Safety evaluation and signal detection
  • Cross-functional matrix team leadership
  • Clinical development and post-marketing safety
  • Regulatory submission safety leadership
  • Safety governance and escalation

Nice-to-have

  • Coaching and mentoring skills
  • Strategic thinking and problem solving
  • Excellent communication and influencing
  • Process improvement and inspection readiness
  • Ability to work in large matrix organizations

Key Requirements

  • PharmD/PhD preferred or BSc Life/Medical Sciences minimum
  • 10+ years pharmaceutical or biotech pharmacovigilance experience
  • Experience with international pharmacovigilance regulations
  • Experience in clinical and post-marketing safety evaluation
  • Experience working in large matrix organizations

Work Rights

Not specified

Tailored Resume

Cover Letter