Very Urgent Requirement for Executive – Pharmacovigilance/ Drug Safety/ Pharmacology/ Drug Regulatory Affairs/ DRA Executive for Delhi Location

M Pharma should be in Pharmacology.

Job description
Responsible for providing medical and clinical insight and guidance through clinical trials for pharmaceuticals.
Primary Responsibilities
Provide medical and clinical guidance to managers before, throughout, and following clinical trials.
Maintain consistency of safety assessments.
Perform a variety of safety assessments.
Serve in cross-functional teams as a medical and scientific representative.
Ensure regulatory compliance and safety throughout trial.
Submit periodic reports to the Food and Drug Administration.
Ensure that medical and causality assessments of all clinical and post-marketing adverse event fillings to foreign regulatory
*Lesioning with FDA (state) & CDSCO; Artwork preparation & Approval; Documents preparation & Review; Dossier Compilation: CTD,ACTD Format; Administrative Documents Preparation.

Role Healthcare & Life Sciences – Other
Industry Type: Pharmaceutical & Life Sciences
Functional Area: Healthcare & Life Sciences
Employment Type: Full Time, Permanent
PG: M. Pharma in Pharmacology Salary Depends on knowledge and experience

Share your CV at at hr@rihimpharma.com