SAB BIO in the United States seeks an Executive Director, Pharmacovigilance to lead global late‑phase safety programs for biologics. This senior IC and team leader role has end-to-end accountability for PV activities supporting regulatory submissions and risk management across the globe. You will oversee signal detection, safety data processing, ISS/ISE preparation for BLA/MAA, CSR safety sections, PSURs, DSURs, and REMS, and you will mentor a PV team while ensuring compliance with ICH and

Also on the board Same function, level within a rung

Level

Manager

Location

New York, NY

Occupation

Regulatory Affairs Managers

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

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