Part-Time On-Site Pharmacovigilance Physician with NIH/NIAID - Long-Term Contract Position - Kelly Government Solutions - Bethesda, MD
Kelly Government Solutions 8 reviews - Maryland

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***Please note this position is not eligible for enrollment in medical and dental benefits and does not offer the opportunity to work remotely***

Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Kelly Government Solutions offers administrative, IT, engineering, scientific, and healthcare professionals the opportunity to work with one of the most prestigious research organizations in the world. We are currently seeking an On-Site Pharmacovigilance Physician to work with the National Institutes of Health in Bethesda, MD.

TASKS/SERVICES: The contractor shall:
(1) Assist in the design and implementation of Phase I-IV clinical trials of vaccines, therapeutics, and other interventions against cholera, anthrax, dengue, West Nile virus, and other microorganisms being studied by the Division

(2) Review, comment on, and accept or reject for implementation clinical protocols for Phase I-IV clinical trials of vaccines and therapeutics for infectious diseases

(3) Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments

(4) Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts

(5) Meets with the Office of Clinical Research Resources (OCRR) Director and staff on a regular basis to provide oral and/or written reports and status updates of on-going projects and to receive new assignments

(6) Provides assistance on a variety of special projects

(7) Attendance at meetings and teleconferences with staff

REQUIREMENTS: The contractor must have:
(1) Medical degree from an accredited university

(2) Active medical license to practice medicine in the US or other country

(3) Experience in evaluating adverse events

(4) Minimum of ten (10) years of experience in medicine or related field

(5) Demonstrates expertise in performing medical research

(6) Demonstrates expertise in developing clinical trial protocols

(7) Demonstrates superior medical writing skills

(8) Knowledge and experience in designing, reviewing and conducting (as either a PI or from the Sponsor perspective) vaccine, therapeutic, or diagnostic clinical trials for treatment/prevention/diagnosis of infectious diseases

(9) Ability to identify gaps in available information and design appropriate trials/studies to fill the gaps

(10) Ability to communicate and defend complex scientific issues orally and in writing

(11) Ability to work in teams and forge consensus

(12) Ability to manage multiple projects and competing priorities

Interested candidates should submit resumes to Susan LoCurto Schechter, Scientific Recruiter, at

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