Executive

Designation: Executive (Aggregate reports and Risk Management) Office Location: Mahape, Navi Mumbai Position description: The Aggregate report and risk management group within Glenmark Global Pharmacovigilance (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 Aggregate report and risk management team works to ensure that Glenmark is compliant with global legislation and guidelines that govern the development, registration and commercialization of its medicines. The Aggregate report and risk management scientist is responsible for preparation of aggregate reports, risk management plan and to keep an oversight on risk minimization activities and risk management plans of Glenmark products. Primary Responsibilities: 1. Authoring of aggregate reports and risk management plans (RMPs). Keeping oversight on risk management activities. 2. Review of risk management plans. 3. Respond to regulatory authority/healthcare professionals queries for assigned products. 4. Review literature search results for ICSRs and articles for inclusion in safety reports. 5. Liaise and collaborate with other GPV functions, international Glenmark affiliates and external business partners. 6. Support audits, inspection and CAPA management relating to Aggregate report and risk management plans ensuring audit requests completed on time. 7. Provide technical guidance in the development and maintenance of procedural documentation. 8. Compliance activities for in-house activities. 9. Ensuring CAPA/deviation are completed on time. 10. Maintenance of PSMF data for aggregate and risk management team. Educational qualifications preferred Degree: Bachelors in Pharmacy and Masters in medicinal chemistry Required work experience Years of experience: Total 3+ years of experience in PV especially in Risk Management Plans, and aggregate reports. Good understanding of drug development process and drug safety regulatory requirements (EU, US regulations as well as ICH and GCP Guidelines) Required Knowledge & Skills : Excellent written and verbal communication including presentation skills Fluent in medical terminology Ability to prioritize and multi-task successfully in a fast paced environment• Ability to interpret and follow regulatory guidelines Ability to react constructively in a high-energy and fast paced environment• Ability to work autonomously, as well as act as a strong team player Excellent interpersonal, analytical, negotiation, decision making and problem solving skills Ability to establish and maintain transparency within the organization and with authorities.

• Experience: 3+ years
• Seniority: Mid Level
• Education: Bachelor's degree preferred
• Languages: English