Associate Director, Global Clinical Safety Scientist
Madrigal Pharmaceuticals · Conshohocken -, PA
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Madrigal Pharmaceuticals seeks an Associate Director of Global Clinical Safety to support pharmacovigilance and safety assessments for clinical products. The role involves coordinating safety activities, analyzing clinical data, contributing to regulatory submissions, and collaborating across functional teams within a biopharmaceutical company focused on metabolic liver disease.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Minimum 10 years clinical safety or pharmacovigilance experience in pharma/biotech
- Bachelor's degree in relevant scientific discipline; advanced degree preferred
- Strong analytical and critical thinking skills with detailed-oriented work
- Knowledge of global safety regulations, MedDRA, and WHO Drug terminology
- Experience with regulatory submissions, safety reports, and safety databases
- Ability to interpret medical records and work within cross-functional teams
- Experience with clinical trial EDC systems and safety process improvement
What you'll be doing
- Serve as safety scientist, coordinating clinical safety activities and escalating complex matters
- Author and review safety sections of protocols, ICFs, and Investigator's Brochures
- Evaluate and summarize clinical safety data to support DRCs, DMCs, and CSRs
- Contribute to regulatory submissions and safety sections of INDs, NDAs, and MAAs
- Identify and evaluate safety signals from clinical trials; prepare responses to regulatory inquiries
Privacy & handoff
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