PWe are currently looking for an experienced strongSafety Physician /strong to support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise across strongClinical Safety and Pharmacovigilance /strong, contributing both operationally and strategically. /ppbr/ppstrongKey responsibilities will include: /strong /pulliProviding comprehensive safety oversight across early- and late-stage development programs /liliAuthoring and reviewing the pharmacovigilance sections of Investigator’s Brochures /liliDeveloping and maintaining risk management plans and associated safety documentation /liliConducting signal detection, evaluation, and ongoing risk management activities /liliSupporting responses to questions and requests from global health authorities /liliPreparing, reviewing, and contributing to key clinical and safety documents, including CSRs, ICFs, CSPs, IBs, and DSURs /liliPerforming narrative reviews, evaluation of SAEs and AESIs, database reconciliation, and related safety activities /liliDefining and driving safety strategy for early clinical development programs /liliCollaborating closely with cross-functional clinical trial teams on critical safety topics /liliProviding strategic input into pharmacovigilance activities and coordinating with both internal teams and external partners /li /ulpbr/ppstrongMandatory Requirements: /strong /pulliMust have MBBS or MD as an educational background. /liliMust have 7 years of Drug Safety experience, that in the clinical trial environment. /li /ulpbr/ppThis role offers the opportunity to play a critical part in shaping and executing safety strategy across the clinical development lifecycle. /p