Clinical Trials Research Nurse Medical Science & Computing (MSC) is an exciting growth oriented company, dedicated to providing mission critical scientific and technical services to the Federal Government. We have a distinguished history of supporting the National Institutes of Health (NIH) and other government agencies. MSC offers a dynamic and upbeat work environment, excellent benefits and career growth opportunities. We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, Medical and Flexible Spending Accounts, Pre-Tax Transit Assistance and tuition reimbursement. If you enjoy being a part of a high performing, professional service and technology focused organization, please apply today! We are currently searching for a Clinical Research Nurse to provide support to the National Institutes of Health (NIH). This opportunity is a full-time position with MSC and it is on-site in Bethesda, Maryland. Duties and Responsibilities: Provide clinical care and direct nursing support for human microbiome outpatient research programs at the National Institutes of Health. Document patient care via established guidelines. Assess, plan and follow up with disease noted attributes. Coordinate various activities (research subject schedules, data and biospecimen collection, and nursing care) to ensure proper and timely filing of standard clinical/regulatory documentation, serious adverse events, amendments, annual reports, and other regulatory documents. Recruit and enroll research subjects. Develop patient rapport and assist in explaining the protocol and tests/procedures to the patients. Consult with health care professionals regarding medical, psychological, and/or social patient needs. Work with medical staff on skilled procedures. Order protocol-mandated tests, labs, and procedures. Distribute biospecimen kits, coordinate biospecimens for testing and diagnostic and research purposes (including referring MDs, NIH labs and repositories) and log biospecimen samples in appropriate database. Follow subjects between visits; collaborate with community physicians to further the continuity of care and protect the integrity of the clinical research protocol/data. Serve as liaison between clinical and laboratory sites, and with Principal Investigators (PIs). Work with staff on clinical research protocol development. Work with staff to develop procedure manuals for clinical research protocols. Work with staff to create case report forms. Visit off-site collaborative centers. Oversee ongoing protocol operations to ensure study compliance; troubleshoot possible protocol violations. Assist in maintaining current regulatory documentation from numerous ongoing clinical research protocols. Interface with relevant Institutional Review Boards (IRB); coordinate filing of UPs, AEs, amendments, continuing review applications, annual reports, protocol inactivation, and other regulatory documents. Assist in the management of research subject files, copying and organizing research data. Assist in updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good Clinical Practices and quality assurance education. Collaborate with PIs to interpret research data for protocol team. Assist investigators and medical writers on the production/revision of clinical research protocols Support the needs of data integrity and retrieval. Participate in quality improvement and quality assurance initiatives involving database and data system development efforts. Assist in the identification of the responsible party for data input into ClinicalTrials.gov at study conclusion, as applicable. Participate in efforts to ensure scientific quality and human subject's protection. Interact with auditing and monitoring agencies to facilitate the exchange of data. Interface with the other protocol support personnel. Position Requirements: . Bachelor's degree in Nursing with current state nursing license. . Minimum of five (5) years of nursing experience with CPR certification. . Experience in a clinical research environment. . Knowledge of clinical research data collection and clinical data report preparation. . Working knowledge of ICH-GCPs. . Knowledge of the principles, theories, techniques and practices of general nursing. . Demonstrated expertise in data management. . Knowledge of Microsoft Office Suite (MS Word, Excel, Outlook) and other spreadsheet applications. . Strong communications skills, both oral and written. . Excellent analytical, organizational and time management skills. Medical Science & Computing is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.