THE LARGEST COLLECTION OF JOBS ON EARTH
pharmaceutical
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
... well as other Worldwide Patient Safety colleagues as well as external ... Affairs, Regulatory Operations, Worldwide Patient Safety, U.S. REMS, and Legal) to ... to support aRMM/REMS regulatory submissions..
... will work with Celgene teams (Safety, Submission, etc.) and the overarching ... multidisciplinary RMP/REMS stakeholders (Submission teams, Lead Safety Physicians, Regulatory Affairs, Biostats, Regulatory ... document requirements, etc.) Support..
... results. Summary The Clinical Trial Lead works with stakeholders across the ... trials that meet ethical, scientific, safety, regulatory, and commercial objectives. The ... commercial objectives. The Clinical Trial..
... a division of Worldwide Patient Safety (WWPS). The Associate Director, contributes ... adoption of new approaches to pharmacovigilance & risk management. The individual ... implement innovation initiatives. Management and..
... Are you looking for a pharmacovigilance role that allows you to ... provide YOU the opportunity to lead key activities to progress YOUR ... include some of the following:..
... Manager, Document Management SUPERVISOR GRM Lead, Publishing and Support DEPARTMENT Center ... Medical Communications/Medical Affairs, Regulatory, or Safety/Pharmacovigilance. REMS and Risk Management Plan ... reports directly to the GRM..