Global Safety Director, Obesity

Jobgether

1d • $189,957 - $246,202 • Remote

About The Position

The Global Safety Director, Obesity will lead the safety strategy for assigned products within the obesity therapeutic area, ensuring patient well-being and regulatory compliance throughout the product lifecycle. This role involves overseeing the global safety profile, managing cross-functional teams, and providing expert guidance on clinical development, risk management, and regulatory submissions. The successful candidate will coordinate safety signal assessments, periodic safety reporting, and inspection readiness initiatives while driving alignment across Safety, Clinical, Regulatory, and Executive teams. You will have the opportunity to influence key product decisions, mentor safety teams, and contribute to strategic planning in a dynamic, fast-paced environment. Occasional domestic and international travel may be required, and remote work is supported.

Requirements

• Doctorate degree with 4+ years of safety experience, or Master’s degree with 7+ years, or Bachelor’s degree with 9+ years
• Expertise in product safety within the biopharmaceutical industry or regulatory environment
• Knowledge of obesity, metabolic, or cardiovascular therapeutic areas, with clinical training preferred
• Experience with marketed product safety, risk management, and Phase 1–3 clinical trial safety assessments
• Demonstrated experience with regulatory submissions, interactions, and compliance reporting
• Leadership experience managing safety profiles and cross-functional teams
• Strong analytical, communication, and strategic planning skills
• Ability to work effectively in a fast-paced, dynamic environment with a global focus

Responsibilities

• Establish and execute global pharmacovigilance strategy and priorities for assigned obesity products
• Lead the Safety Analysis Team (SAT) and Global Safety Team (GST) and participate as a core member of the Executive Safety Committee (ESC)
• Validate safety signals, conduct safety assessments, and develop mitigation strategies
• Prepare and review core safety information, risk management plans, and periodic aggregate safety reports
• Provide safety input for clinical protocols, statistical analysis plans, and study reports
• Author and review safety sections of regulatory submissions, including new drug applications
• Serve as safety expert on cross-functional Evidence Generation Teams, supporting clinical and commercial initiatives
• Ensure inspection readiness and compliance with domestic and international safety regulations

Benefits

• Competitive base salary range of $189,957–$246,202 annually, subject to experience and qualifications
• Comprehensive health, dental, and vision coverage for employees and eligible dependents
• Retirement and savings plans with employer contributions
• Annual discretionary bonus program and potential stock-based incentives
• Award-winning paid time off and flexible work arrangements
• Professional development opportunities and career growth support
• Support for work-life balance and employee well-being programs

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree