Overview Must be a US Citizen or Green Card Holder W2 with full benefit Some travel may be required. Offer contingent on ability to successfully pass a background check and drug screen. Eligible for some Telework. 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 Research 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 . The US base salary for this full-time position is $52-60/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 The primary role for this Research Coordinator (RC) position is to provide clinical research coordination and protocol navigation for the NINDS Intramural Research Program. Supports clinical staff develop, implement and maintain clinical research data files and materials. Collects research data and prepares information for inputs and analysis. Supports the development of forms and questionnaires. Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests. Monitors subject's progress and reports adverse events. Supports assembly, development and review of new research projects. Supports the creation and management of clinical websites and web-based tools. Organizes and performs clinical research, utilizing internet and other available clinical resources. Provides assistance to staff in the collection, development and quality control of essential clinical research efforts. Develops and facilitates training to new research coordinators and mentors researchers in Good Clinical Practices. Qualifications Required Skills: Bachelor’s degree in biology or a health-related field. Preferred Software: Clinical Trial Management System (CTMS), Electronic Medical Records System, Electronic Data Capture System. Certifications and Licenses: Association of Clinical Research Professionals Certified Professional (ACRP-CP), Association of Clinical Research Professionals (ACRP), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA). Experience with the following: Overseeing and documenting IP dispensing, inventory and reconciliation. Closing clinical trial sites down on completion of clinical trial. Ordering, tracking, and managing IP and trial materials. Implementation of clinical trial site action plans. Training clinical trial site staff. Coordinating project meetings. Previous clinical trial work. Electronic medical records. Protocol review revision. Phase I or II experience. Patient confidentiality. Remote site monitoring. Regulatory compliance. Protocol development. Clinical Research. Protocol writing. Clinical Trials. Data Monitoring. Data Integrity. Patient care. Recruitment. Scheduling. Screening. Research.
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