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| Job Location | Bangalore |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Management Consulting / Strategy |
| Functional Area | Pharmacist / Medical Representative |
| EmploymentType | Full-time |
IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.Medical evaluation of individual adverse event case safety reports, including but not limited to all serious, non serious line listings, expedited reports and all pregnancy reports. Accountable for review and interpretation, analysis and summarization of aggregate safety data from all sources including spontaneous, clinical, post-marketing and observational studies, literature review and product quality, (e.g. RMP, PSUR, ad-hoc regulatory reports, etc) Ensuring service delivery from productivity, compliance and quality perspective. Lead and participate in the initiatives taken for the same from team delivery perspective Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing a Pharmacovigilance Physician product team and/or technical leadership in single case assessment. Ensuring updation of watch list, labeling list/RSIs etc for the assigned products and develop such additional capabilities within the team Responsibilities include lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives Participate in signal detection efforts, e.g. strategy meetings for PSURs and periodic reports and structured surveillance programs and execution of pharmacovigilance components of Risk Management Programs and related activities including assessment of potential signals Lead and participate as members of pharmacovigilance matrix-teams responsible for pharmacovigilance activities focused on individual products and therapeutic areas. Responsibilities include training activities, participation in selected reviews of aggregate reports such as PSURs, PADERS, contributing to the development and implementation of risk minimization action plans, as applicable etc Join UsMaking a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.Forge a career with greater purpose, make an impact, and never stop learning.Job ID: R1121051,
Keyskills :
product qualitydata science hseadvanced analytics sitesafety risk managementservice delivery