Job Summary
A company is looking for an Associate Medical Director, PVRM.
Key Responsibilities
- Monitor and assess risks/benefits for investigational and marketed products throughout their lifecycle
- Conduct safety surveillance, reviewing clinical trial and post-marketing safety reports
- Generate and evaluate safety data, contributing to various safety documentation and reports
Required Qualifications
- Medical Degree (MD) with 3-5 years of drug safety experience in a pharmaceutical company
- Experience in Oncology and Neurology is preferred
- Advanced understanding of pharmacovigilance and risk management regulations
- Expertise in medical review of individual case safety reports and aggregate safety reports
- Knowledge of drug development and global regulatory requirements
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