Pharmacovigilance - SERM

4 - 6 years

3.0 - 8.0 Lacs P.A.

Navi Mumbai, Mumbai (All Areas)

Posted:3 months ago| Platform: Naukri logo

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Skills Required

Pharmacovigilancesignal detectionsignal management activitiesDrug safety reportsbenefit risk reportsRisk management plansSERMSafety evaluation Risk Management

Work Mode

Work from Office

Job Type

Full Time

Job Description

Role Brief: Incumbent will be a part of the SERM team, working on SERM related activities. The Safety Evaluation and Risk Management (SERM) group within GPV is responsible for the scientific evaluation of safety information and the continuous monitoring of the benefit-risk profile of all Glenmark products throughout all stages of the product lifecycle. The SERM works to ensure that Glenmark is compliant with global legislation and guidelines that govern the development, registration and commercialization of its medicines. The SERM scientist is responsible for all safety evaluation and risk management activities for Glenmark products including (but not limited to) the preparation of safety reports, risk management plans and signal assessments. Role & responsibilities: 1) Author/ review/ approve drug safety reports 2) Contribute to the development and implementation of Risk Management Plans 3) Perform signal detection, evaluation and overall signal management activities 4) Lead or participate in cross-functional safety review teams for products in clinical development 5) Review and provide input into safety sections of study related documents 6) Respond to regulatory authority/healthcare professionals queries for assigned products 7) Review literature search results for ICSRs and articles for inclusion in safety reports 8) Liaise and collaborate with other GPV functions, international Glenmark affiliates and external business partners 9) Support product labelling activities 10) Support audits, inspection and CAPA management relating to SERM activities 11) Support assessment and implementation of regulatory intelligence findings that impact SERM activities 12) Provide technical guidance in the development and maintenance of procedural documentation 13) Support organizational initiatives in driving global operational excellence in Pharmacovigilance 14) Support the EEA QPPV 15) Clinical Trial support 16) Vendor Management 17) Website Monitoring Preferred candidate profile : 4 + years of experience within PV & SERM M.Pharm preferred

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