Qualification: M Pharm (Pharmacology) or BAMS and BDS
1-2 years of experience in handling the pharmacovigilance activities (Consumer and Clinical Research) of Drug Products and Biologicals Prepare, review and submit the Periodic Safety Update Reports and other clinical related applications to regulated and semi regulated Markets.
Clinical Dossier Management & Technical Writing
If you think you are a fit or match reach out to us on: Email: cv@pharmaleaf.com
