Clinical Trial Safety Physician - NIH

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 the leading medical research center in the world. We are seeking an individual to work as a Clinical Trial Safety Physician at the National Institutes of Health. Position estimated to support a hybrid work arrangement that includes mostly remote work with occasional on-site work at the NIH in Rockville, MD for meetings and related activities. This is a long-term contract position which offers:

• Competitive compensation and comprehensive benefit package
• Optional health, vision, and dental plans
• Vacation leave as well as paid federal holidays and 401K plan.
• Access to NIH’s unparalleled resources and niche scientific initiativesTASKS/SERVICES. The contractor shall:

• 1) Review pharmacovigilance reporting strategies (e.g., safety monitoring plans), incoming safety data (e.g., adverse event reporting, safety committee’s reports), review of clinical study reports, investigator brochures, advisory committee recommendations, package inserts, and scientific literature.
• 2) Work with staff on clinical protocol development, including providing input on study safety design (e.g., study objectives, subject safety, safety reporting), conducting reviews of clinical protocols and all supporting documents, and providing feedback to DMID staff and clinical investigators.
• 3) Provide clinical expertise in the areas related to infectious diseases to Division of Microbiology and Infectious Diseases (DMID) staff and make recommendations about key clinical issues.
• 4) When needed make recommendations and/or discuss clinical design and safety issues with representatives from various groups (e.g., DMID colleagues, industry representatives, contractors, grantees, and safety monitoring committee members) either by a written report or through discussion and/or presentation.
• 5) Develop and maintain a proficiency in accessing and reviewing clinical study related information from databases used by DMID.REQUIREMENTS. The contractor must have:
• 1) Medical degree (MD) from an accredited university
• 2) Minimum of ten (10) years of related medical experience
• 3) Experience evaluating adverse events as part of early phase clinical trials
• 4) Demonstrate expertise developing and reviewing clinical trial protocols including input regarding study safety designPLEASE APPLY ONLINE

When you apply, please know a Kelly Government Solutions Recruiter will review your resume and will contact you directly, if your skills and experience match the requirements of this position; a full job description can be made available at that time. Due to the high volume of inquiries, we regret that we cannot accept phone calls. Even if you aren’t contacted for this position, you are still part of our talent network. All Kelly recruiters have access to your profile, which expands your opportunities even further.As a specialty talent company, Kelly is committed to doing the right thing for our talent and clients. We stand up for equity, inclusion, fair treatment, and opportunity for all as these build the foundation of our Talent Promise. With a focus on safety, value, well-being, investment, and opportunity, Kelly’s Talent Promise confirms our commitment to those in search of a better way to work and live and to help discover what’s next.It is obvious things are different than they were just a few months ago. Kelly is at the forefront of ensuring the safety of our employees in this new working environment. Be well and stay strong. #government9470794 Rockville, MD, US Scientific Doctorate/PhD Full Time, Temporary Experienced (Non-Manager) On-site Government and Public Sector First Shift (Day)