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Sr. Director of Drug Safety Risk Management. Prior experience in drug safety and risk management is strongly preferred. Support regulatory submissions, including applications for marketing authorization and new drug/biologic licenses.
$250,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist the Medical Safety Assessment (MSA) TA Head/Lead in developing and maintaining state-of-the-art Pharmacovigilance (PV) processes and procedures within BMS Drug Development and WWPS.· Support the EU Qualified Person for PV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
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The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle.
$284,375 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Working knowledge of validated drug safety databases (preferably ARGUS) and MedDRA. Highly-developed scientific and analytical knowledge base and an excellent understanding of good pharmacovigilance practices and current regulations within drug safety.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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The position reports to the Director, Global Drug Safety & Pharmacovigilance, Scientist Lead. As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members.
$237,500 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Experience in regulatory requirements and guidelines pertaining to Drug Safety and Pharmacovigilance are required. Prior experience with Drug Safety and Risk Management strongly preferred.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Train drug safety associates and contribute to mentoring and on-boarding of new colleagues. Partnership with Global Clinical Development Project Leaders on Program Development from Phase I to life cycle regarding safety and risk- benefit topics and decisions including contribution and review of new drug approval filing documents.
Full-timeExpandApply NowActive JobUpdated 24 days ago
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