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To establish and lead U.S. pharmacovigilance operations, the full-time Associate Director, Pharmacovigilance will manage client-facing programs, develop operational processes, and collaborate with global teams in a remote capacity.
Key Responsibilities: Establish and develop the operational structure and processes for U.S. pharmacovigilance services Independently manage pharmacovigilance projects, ensuring compliance and quality throughout the project lifecycle Provide technical oversight for safety reporting activities and collaborate with cross-functional teams for coordinated safety oversightRequired QualificationsBachelor's degree or higher in Pharmacy, Medicine, Nursing, Life Sciences, or a related field At least 8 years of experience in pharmacovigilance or drug safety, with a focus on clinical development programs Strong knowledge of FDA pharmacovigilance regulations and ICH guidance Experience in managing pharmacovigilance projects with a focus on client communication and operational oversight Hands-on understanding of safety case processing and regulatory reporting

Also on the board Same function, level within a rung

Level

Manager

Location

New York, NY

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

2 days ago

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