Associate Medical Director, Medical Safety

This position is posted by Jobgether on behalf of a partner company. We are currently looking for an Associate Medical Director, Medical Safety in United States.

This role offers a unique opportunity to shape the safety strategy of innovative therapies across their full lifecycle. As a key medical expert within pharmacovigilance, you will oversee the benefit-risk profile of both investigational and marketed products, ensuring patient safety remains at the forefront of development and commercialization efforts. You will collaborate closely with cross-functional teams and external stakeholders, influencing regulatory submissions and clinical strategies. The position combines scientific rigor with strategic decision-making in a fast-paced, global environment. It is ideal for a physician who thrives on translating complex safety data into actionable insights. You will play a critical role in safeguarding patients while supporting the advancement of life-changing treatments.

• Lead and support global safety strategy implementation for assigned products across clinical development and post-marketing phases
• Conduct signal detection, evaluation, and interpretation using individual and aggregate safety data, ensuring timely communication of risks
• Author and review key safety documents including PSURs, PBRERs, DSURs, regulatory submissions, and clinical study reports
• Collaborate with cross-functional teams (clinical, regulatory, biometrics, medical affairs) to ensure alignment on safety strategy and execution
• Contribute to risk management planning, including development and maintenance of core safety information and product labeling
• Participate in and lead safety governance forums, including Safety Management Teams and advisory committees
• Ensure compliance with global pharmacovigilance regulations and support audit and inspection readiness activities

Requirements:

• MD (or equivalent) required; medical licensure preferred, with specialization in internal medicine, oncology, neuroscience, or related field considered a plus
• Minimum of 3 years’ experience in pharmacovigilance, drug safety, or clinical development within the pharmaceutical or biotech industry
• Strong knowledge of global pharmacovigilance regulations and guidelines (FDA, EMA, ICH, CIOMS)
• Experience with safety databases and coding systems such as MedDRA and WHODrug
• Proven ability to analyze and interpret complex clinical and safety data
• Strong communication and collaboration skills, with the ability to work effectively in cross-functional environments
• Highly organized, self-driven, and capable of managing multiple priorities in a dynamic setting

Benefits:

• Competitive salary range ($212,000 – $318,000) with performance-based bonus opportunities
• Equity incentives and long-term compensation plans
• Comprehensive healthcare coverage including medical, dental, and vision insurance
• 401(k) retirement savings plan with company participation
• Flexible paid time off and vacation policy
• Opportunities for career development and continuous learning
• Remote work flexibility and global collaboration environment