The Clinical Trial Reviewer is a full-time physician position with the FDA. It is a hybrid role where candidates must live within commutable distance of the FDA Headquarters in Silver Spring, MD and willing to report to the office at least one day per week. The team follows traditional working hours with no overtime or weekend hours.
A Day in the Life:
As an oncology expert for the FDA, you will review new drugs to ensure that they’re safe and effective.
- Before testing on humans: You will check if the drug’s design is sound.
- For approval: You will evaluate clinical trial results and labeling accuracy to ensure the drug works as intended and has clear instructions and warnings.
- For existing drugs: You will review updates, safety reports, and potential new uses or label changes.
You will work with your team to make evidence-based decisions.
- You will analyze summaries from other experts and recommend approving, requesting more data, or rejecting applications.
- You will consult with other specialists to address complex issues and stay up to date on scientific advancements.
- You will share your expertise through conferences and publications.
Position Requirements:
Education:
- US or Canadian Medical Degree: MD, DO, or equivalent from an accredited school.
- Foreign Medical Degree: MD or equivalency, such as a ECFMG certification or USMLE completion.
Licensure:
- Current, active, full, and unrestricted medical license in the US or its territories.
Needed Experience:
- Ability to apply clinical and scientific knowledge to complex medical problems and benefit/risk management.
- Enjoys solving unique problems and addressing challenges in drug/biologic regulatory review.
- Desire to stay current on the latest clinical information in your assigned therapeutic area.
- Capable of strong written and verbal communication.
AE Strategies has provided human capital management consulting to federal clients for the past 20 years. We are proud to be partnered with the FDA to assist with their recruiting needs.
