Senior Medical Officer - Pharmacovigilance & Drug Safety for onsite opportunities in
Rockville, MD. Package includes competitive rates and long-term federal contract opportunities.
Job Description:- Provides medical safety oversight for DMID-sponsored clinical trials.
- Reviews clinical trial protocols for safety and operational issues.
- Assesses Serious Adverse Events (SAEs) and reviews SUSAR notifications.
- Performs medical data reviews, including laboratory values, adverse events, coding, tables, listings, and figures.
- Represents DMID in communications with the FDA, sponsors, and academic partners.
- Serves as a safety expert on safety committees.
- Develops safety-related policies and guidelines.
- Identifies process gaps and supports issue resolution.
Required Qualifications & Documentation:- MD from an accredited university.
- Minimum 10 years of relevant experience.
- U.S. work authorization required (No visa sponsorship).
- No security clearance required.
- Experience in Pharmacovigilance, Drug Safety, Medical Monitoring, or Sponsor/CRO safety monitoring preferred.
