Major Purpose of the Job: Single Point of Contact for all Pharmacovigilance activities for International (Formulation) business.
Principal Accountability: Doing research work on adverse events or product complaints or with an inquiry about the human health product;
Receiving calls from consumers and health care professionals with reports and respond to inquiries;
Verbal Probing for necessary information including but not limited to the adverse event(s),
the patient's medical history, Suspect product, concomitant drugs involved if any, and medication history
of patient;
To be responsible to the Medical Head for day-to-day processing of incoming adverse event reports and reporting to regulatory authorities, with the objective of achieving a high level of regulatory compliance;
To ensure that all Pharmacovigilance activities are conducted in accordance with SOP's, Work Instructions, Good Clinical Practice guidelines and regulatory requirements;
To assist the Medical Head in preparation for any internal audits or external inspections on CPL Pharmacovigilance function;
To liaise with Clinical Research personnel in the preparation of safety data required in support of the clinical research program.
Salary: Not Disclosed by Recruiter
Industry: Pharma /
Biotech /
Clinical ResearchFunctional Area: Medical,
Healthcare,
R&D,
Pharmaceuticals,
BiotechnologyRole Category: Medical Officer
Role: Medical Officer
Experience : 2 - 5 Years
Location: Ahmedabad
Keyskills: pharmacovigilancepharma covigilancepharmaceutical covigilancemedical covigilance