Senior Medical Safety Advisor

Role: Senior Medical Safety Advisor Total Experience: 5+ Years. Pharmacovigilance/PV Experience : 1+ Years Work location & Mode : PAN India -Homebased Education : MBBS/MD Graduates. The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products. Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary ~ Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements ~ Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications, or other medical data listings to verify and medically vet clinical data ~ Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported ~ Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable ~ Provide aggregate reviews of safety information, including but not limited to clinical data, post marketing, literature review and observational studies to maintain oversight of a product’s safety profile (e.g: DSUR, RMP, PBRER, ad hoc regulatory reports etc) ~ Ensure service delivery from productivity, compliance and quality perspective within regulatory /contracted timelines. Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in single case assessment. ~ Lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives ~ Review and sign off on the Project Safety Plan and Medical Monitoring Plan per medical safety scope agreed in contract, as applicable ~ Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable ~ Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable ~ Provide medical escalation support for medical information and EU Qualified Persons for Pharmacovigilance projects, as applicable ~24-hour medical support as required on assigned projects ~ Maintain awareness of medical safety-regulatory industry developments ~ MBBS OR MD from an accredited and internationally recognized medical school with a curriculum relevant to general medical education is required. ~1+ years of pharmacovigilance experience and 5+ years of total experience is mandatory. ~ Sound knowledge of Medicine ~ In-depth knowledge of applicable global, regional and local clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ~ Skill in use of multiple safety databases ~ Adequate Computer skills, especially Microsoft word, excel & PowerPoint ~ Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients and regulatory agency representatives ~ A valid medical license, or equivalent, from the country or region in which he/she resides and works preferred.