Senior Medical Director, PVRM
reputed company
The Pharmacovigilance and Risk Management (PVRM) Senior Medical Director will be responsible for the medical safety aspects of clinical trials, including review and assessment of individual case safety reports, and providing medical safety subject matter expertise in the review and approval of documents.
What You Will Do
reputed company safety reputed company and key messaging in NDA/BLA/MAA submissions, reputed company PVRM Medical representation on product specific and/or clinical study team meetings and governance committees, and prepare and present safety data analysis to project teams and senior management.
Why It Might Be a Fit
This role requires a thorough knowledge of the reputed company industry, especially clinical research and global regulatory requirements, and experience managing expedited and periodic safety reporting, signal reputed company, safety evaluation and risk management strategies.
Requirements
- Medical Degree (MD) with 12 + years of relevant experience in biotech or pharmaceutical industry
- Experience in Oncology and Neurology is preferred
- Experience with NDA/BLA/MAA submission
- Prior people management experience
Benefits
- reputed company-based salary increases
- Short incentive plan participation
- 401(k) plan
- Medical, dental, reputed company, life and disability insurances
- Leaves provided in line with your work state
- Flexible reputed company time off
- 11 reputed company holidays
- Additional time off for a shut-down period during the last week of December
- 80 hours of reputed company reputed company time upon hire and reputed company year thereafter
Originally posted on Himalayas
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