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.