Analysis Skills, Background Investigation, Clinical Outcomes, Clinical Practices/Protocols, Clinical Study Publications, Clinical Trial, Database Administration, Electronic Medical Records, Federal Government, Genetics, Genomics, Healthcare, Information Technology & Information Systems, Medical Record System, Medical Research, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Operations Processes, Organizational Skills, Patient Care, Patient Confidentiality, Patient Education, Regulations, Research & Development (R&D), Staff Training, Technical Research, Technical Support, United States Citizen, Vendor/Supplier Planning
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
- Learn more about what Columbus can do for you at www.columbususa.com
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).
- Assists researchers with protocol development, assembly and review of clinical trial documents.
- Assists researchers develop and maintain trial related documents and operational procedures.
- Maintains study databases and conducts basic analysis.
- Assists researchers collect, distribute and file regulatory documents.
- Provides technical support to researchers and the clinic.
- Develops and assembles clinical trial documents.
- Develops and maintains trial related documents and operational procedures.
- Collects and distributes regulatory documents.
- Develops, assembles and reviews clinical trial documents.
- Collects, distributes and files regulatory documents
- Reviews and recommends changes to clinical trial documents.
- Reviews and maintains trial related documents and operational procedures.
- Collects, distributes and submits regulatory documents.
- Develops training plans and trains 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 be understanding of patient confidentiality