1+ months

Advancing Therapeutics Development for Pregnant and Lactating Patients: U.S. Food & Drug Admin.

Silver Spring, Maryland
  • Job Code
    source code: #20-088EG
  • Job Type

Advancing Therapeutics Development for Pregnant and
Lactating Patients

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 (FDA), Center for Drug Evaluation and Research (CDER), Office of New Drugs (OND) 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 Pediatric and Maternal Health within OND is seeking highly qualified physicians to serve as clinical reviewers. We are seeking individuals who are board certified or board eligible in obstetrics and gynecology, family medicine, preventive medicine, and/or internal medicine. We are particularly interested in individuals with expertise in maternal-fetal medicine and/or teratology as well as interest in epidemiology and/or clinical pharmacology. Graduating fellows and junior faculty are encouraged to apply. 

Primary responsibilities of the clinical reviewer include the following:

  • Determines whether clinical trials of new drugs and therapeutic biologics in humans are soundly conceived and supported to justify human testing
  • Reviews clinical protocols and provides input regarding study design
  • Together with other team members, interacts with investigators and drug companies to guide development of drugs and therapeutic biologics
  • Determines whether marketing applications should be approved based on an evaluation of the evidence of safety and effectiveness
  • Consults, when needed and where appropriate, with other medical specialists and scientists within and outside FDA
  • Assists in the development and conduct of training programs, educational activities, workshops and conferences
  • Keeps abreast of the progress in medical and related sciences by reviewing the scientific literature and participating in staff seminars where cases and topics of interest are discussed 

As a clinical reviewer, you will have the opportunity to:

  • Advance the public health through new drug development;
  • Experience teaching and training opportunities;
  • Interact with pharmaceutical companies, world-renown disease experts, patients and advocacy groups; and
  • Work with a wide range of scientific disciplines in a team-oriented atmosphere.


This position allows for one half-day per week of patient care, if interested. 


  • Salary is commensurate with experience and expertise
  • Excellent federal government benefits package (health insurance, life insurance, retirement, etc.).
  • Relocation expenses and student loan repayment may be paid to eligible candidates.
  • Flexible and/or partial telework schedules available (after completion of initial training period).



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 (ECFMG). 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. 

Please send a current CV/resume and cover letter to
ond-employment@fda.hhs.gov for consideration. Please reference source code: #20-088EG in the subject line.



Posted: 2020-08-06 Expires: 2020-11-04

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Advancing Therapeutics Development for Pregnant and Lactating Patients: U.S. Food & Drug Admin.

Silver Spring, Maryland

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