Senior Director, Global Regulatory Affairs, Oncology

GSK

Senior Director overseeing global regulatory strategy and compliance for pharmaceutical projects at GSK. Leading cross-functional teams to develop and execute regulatory strategies for optimal drug development outcomes.

Posted 5/2/2026full-timeUpper Providence • Massachusetts, Pennsylvania • 🇺🇸 United StatesSenior💰 $222,000 - $370,000 per yearWebsite

About the role

Key responsibilities & impact

Ensure the development of appropriate regulatory strategies and execution for assigned asset(s)
Work with the Early/Medicine Development Team (EDT/MDT) to ensure a robust regulatory strategy is in place
Proactively develop regulatory strategies and promote innovative regulatory approaches
Lead regulatory interactions and the regulatory review processes
Ensure effective interaction with local regulatory counterparts in priority markets

Requirements

What you’ll need

Bachelor’s degree in a biological, life science, or healthcare field
Significant experience in regulatory affairs (10+ years)
5+ years experience across all phases of drug development and regulatory submissions
Track record leading global or regional regulatory strategy and interactions with health authorities
Experience working in complex matrix teams with clinical, CMC, commercial, and safety functions
Strong written and verbal communication skills with ability to present clearly to senior leaders and regulators.

Benefits

Comp & perks

Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation
Paid caregiver/parental and medical leave

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory strategyregulatory submissionsdrug developmentregulatory interactionsregulatory review processes

Soft Skills

communication skillspresentation skillsleadershipcollaboration