Safety Evaluation and Risk Manager Contract | Must Have MBBS or MD | 12 Months
This contract role sits within a global pharmacovigilance function, supporting signal detection, benefit risk assessment, and regulatory reporting across a portfolio of designated products. The successful candidate will work closely with product scientists, clinical development teams, and regulatory stakeholders to maintain safety oversight and ensure compliance with international standards.
Responsibilities:
Lead pharmacovigilance and risk management planning for designated products, including preparation of regional Risk Management Plans and benefit risk assessments
Run routine signal detection processes using signal management tools, literature review, and database searches, and lead data evaluation discussions with TA Directors and key stakeholders
Author and coordinate periodic regulatory documents including PSURs and Annual Reports, ensuring submissions meet agreed timelines and qua...