Job Summary

• This position provides in-depth medical/scientific expertise in the safety evaluation and risk management (SERM) of key GSK assets in clinical development and/or post-marketing setting.
• The role leads the safety component of global regulatory submissions and facilitates safety governance/SRTs in clinical development and post-marketing settings.
• Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

Matching Summary

Salary

Base: $239,250 to $398,750; Bonus/Equity: annual bonus and eligibility for share-based long-term incentive; Benefits: health care, insurance, retirement, paid holidays, vacation, paid leave

Skills & Requirements

Key Requirements

• Medical degree
• Completion of formal postgraduate clinical training
• 5+ years in Pharmaceutical/Biotech in Pharmacovigilance/Drug Safety
• 5+ years pharmacovigilance experience (clinical development & post-marketing)
• 5+ years experience with Signal Detection and safety surveillance

Work Rights