Health Science Policy Analyst

Health Science Policy Analyst

This position is being filled under a streamlined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career‑conditional appointment and be paid under the provisions of this authority.

This position is being recruited based on the Title 21 Pay Table 1, Band D, $143,913 - $197,200.

Basic Qualification Requirements:
Education Bachelor's or graduate/higher level degree: major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position. This degree must be from an educational program from an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained.

• Have a Bachelor's degree and 5 years of relevant experience coordinating and collaborating with relevant program areas to ensure optimal agency scientific and technical input for ongoing policy initiatives in areas pertaining to the development and conduct of clinical trials, risk‑based monitoring, quality by design, and risk paradigms associated with drug development, bioresearch and monitoring, and human subject protection.
• Have a Master's degree and 4 years of relevant experience coordinating and collaborating with relevant program areas to ensure optimal agency scientific and technical input for ongoing policy initiatives in areas pertaining to the development and conduct of clinical trials, risk‑based monitoring, quality by design, and risk paradigms associated with drug development, bioresearch and monitoring, and human subject protection.
• Have a Doctorate degree and 2 years of relevant experience coordinating and collaborating with relevant program areas to ensure optimal agency scientific and technical input for ongoing policy initiatives in areas pertaining to the development and conduct of clinical trials, risk‑based monitoring, quality by design, and risk paradigms associated with drug development, bioresearch and monitoring, and human subject protection.
• Have a MD, DO, DDS, DPM or DVM degree and 2 years of relevant experience coordinating and collaborating with relevant program areas to ensure optimal agency scientific and technical input for ongoing policy initiatives in areas pertaining to the development and conduct of clinical trials, risk‑based monitoring, quality by design, and risk paradigms associated with drug development, bioresearch and monitoring, and human subject protection.

NOTE:

Applicants must submit all relevant transcripts that demonstrate you possess the required education to meet the Basic Qualifications. Applications must be submitted by 11:59 pm EST on 07/24/2026.