Clinical Protocol Coordinator

Overview Must be a US Citizen or Green Card Holder W2 with full benefit Offer contingent on ability to successfully pass a background check and drug screen Columbus Technologies and Services Inc. is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Columbus 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 a Clinical Protocol Coordinator to work onsite with the National Institutes of Health in Bethesda, MD. This is a long‑term position which offers: Competitive salary Tremendous growth opportunity Opportunity to work at NIH, the world's foremost medical research center The US base salary range for this full‑time position is $45-54/hr + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job‑related skills, experience, and relevant education or training. Responsibilities Provide molecular diagnostics and genetic counseling for patients — particularly in communicating high‑impact, actionable results at the Clinical Center, providing direct patient care in the context of research genomic services, which are essential for the safe and uninterrupted continuation of patient clinical treatments under NIAID’s Centralized Sequencing Program (CSP). Assist researchers with protocol development, assembly and review of clinical trial documents. Assist researchers develop and maintain trial related documents and operational procedures. Maintain study databases and conduct basic analysis. Assist researchers collect, distribute and file regulatory documents. Provide technical support to researchers and the clinic. Develop and assemble clinical trial documents. Develop and maintain trial related documents and operational procedures. Collect and distribute regulatory documents. Develop, assemble and review clinical trial documents. Collect, distribute and file regulatory documents. Review and recommend changes to clinical trial documents. Review and maintain trial related documents and operational procedures. Collect, distribute and submit regulatory documents. Develop training plans and train staff on the proper techniques for protocol submission. Qualifications Master’s degree in Genetics or related field of study. Must be certified or board‑eligible as a Genetic Counselor by the American Board of Genetic Counseling. Must be able to be credentialed by the NIH Clinical Center. Experience with Electronic Medical Records System. Must understand patient confidentiality. #J-18808-Ljbffr Columbus Sverige