We are currently looking for an experienced Safety Physician to support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise across Clinical Safety and Pharmacovigilance, contributing both operationally and strategically.
Key responsibilities will include:
Providing comprehensive safety oversight across early- and late-stage development programs
Authoring and reviewing the pharmacovigilance sections of Investigator’s Brochures
Developing and maintaining risk management plans and associated safety documentation
Conducting signal detection, evaluation, and ongoing risk management activities
Supporting responses to questions and requests from global health authorities
Preparing, reviewing, and contributing to key clinical and safety documents, including CSRs, ICFs, CSPs, IBs, and DSURs
Performing narrative reviews, evaluation of SAEs and AESIs, database reconciliation, and related safety activities
Defining and driving safety strategy for early clinical development programs
Collaborating closely with cross-functional clinical trial teams on critical safety topics
Providing strategic input into pharmacovigilance activities and coordinating with both internal teams and external partners
Mandatory Requirements:
Must have MBBS or MD as an educational background.
Must have 7 years of Drug Safety experience, that in the clinical trial environment.
This role offers the opportunity to play a critical part in shaping and executing safety strategy across the clinical development lifecycle.