Are you making an outsized difference to the public health and well-being of Americans? Would you like to? The physicians, scientists and other dedicated professionals at the U.S. Food & Drug Administration, Center for Drug Evaluation and Research, Office of New Drugs located in Silver Spring, MD, contribute to the public health of millions of Americans every day. We pride ourselves on our dedicated and skilled staff and are looking for committed individuals to help us achieve our mission. OND’s mission is to ensure that safe and effective drugs and biologics are available to Americans. We provide guidance to drug companies on a wide variety of clinical, scientific, and regulatory matters and make decisions on whether new drugs or new uses of already marketed drugs should be approved.
The Division of Urology, Obstetrics, and Gynecology within the Office of New Drugs is seeking highly qualified physicians to serve as clinical reviewers to assess drugs and therapeutic biologics for use in urologic conditions in men and women. We are seeking individuals who are preferably board certified or board eligible in urology or urogynecology. Preference will be given to applicants with clinical urology or urogynecology experience including fellows and those retired from clinical practice.
Primary responsibilities of the clinical reviewer include the following:
As a clinical reviewer, you will have the opportunity to:
This is primarily a non-clinical position; there is an option to provide one half-day per week of clinical care, if interested.
SALARY & BENEFITS
QUALIFICATIONS
Applicants must have a Doctor of Medicine or Doctor of Osteopathy degree from an accredited medical school. Graduates of foreign medical schools must be certified by the Education Commission for Foreign Medical Graduates. Candidates must be U.S. citizens. Permanent U.S. residents may apply for staff fellowship appointments. Excellent oral and written communication skills and an ability to work effectively in a team are necessary to be successful in this role. A competitive candidate will have experience working with clinical data with enough knowledge and understanding of clinical trial design to evaluate extensive, long-range scientific programs, and their implications on the drug development process. Prior human subject research experience is desired, but not required.
TO APPLY
Please send a current CV/resume and cover letter to ond-employment@fda.hhs.gov for consideration.
Please reference source code: #22-046EG in the subject line.