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Clinical Research Nurse
2 months ago
Cape Fox Shared Services is seeking a highly skilled Research Nurse to support our team in Bethesda, MD. As a Research Nurse, you will play a critical role in the success of our clinical research studies.
Key Responsibilities:- Recruit and follow patients for clinical and basic research studies on HIV vaccines and emerging/re-emerging vaccines.
- Review charts to collect relevant clinical data, including laboratory test results and social background.
- Interview patients to obtain medical history, sexual history, medication history, and previous HIV-related risks factors.
- Assist research and medical staff in interviewing, screening, and evaluating eligible subjects for participation in research protocols.
- Participate in recruitment and outreach activities, contributing to innovative recruitment strategies.
- Recruit and follow up with patients for clinical and basic research studies, providing clinical support to patients participating in protocols.
- Design and maintain materials for health care referral sources, including eligibility information and other objectives.
- Organize and maintain an active referral list and master schedule for planning follow-up and new patient admissions.
- Provide instruction to potential clinical study subjects and those involved in care on aspects of subject care, treatments, and side effects.
- Communicate study information to referring physicians, advocacy groups, NIH offices, and potential study participants.
- Participate in direct patient care, coordinating with interdisciplinary teams to create and communicate a plan of care balancing clinical care needs with research.
- Obtain and record complete health histories, conduct physical assessments, and communicate data from these and other sources.
- Manage clinical and research support activities to ensure patient safety and address clinical needs.
- Review findings from assessments and other sources in clinical rounds.
- Complete medical and psychiatric assessments of potential participants in multiple research protocols, collecting and reviewing past and present medical records and conducting interviews with research applicants and their families.
- Conduct family interviews to obtain a comprehensive understanding of the care needs of the patient.
- Continually assess ongoing understanding of the research process for patients and families, providing teaching and support as indicated.
- Ensure informed consent process and human subjects protection in clinical research, counseling patients regarding potential risks.
- Collaborate with researchers and medical staff to obtain and maintain informed consent and assent, addressing ethical and legal implications of research protocols.
- Contribute to all study-related IRB and regulatory matters, including reporting requirements and issues.
- Collect and report data to regulatory and monitoring agencies.
- Perform quality assurance and quality control activities relating to protocol adherence, data collection, and data analysis, protecting research participant data in accordance with regulatory requirements.
- Perform accurate data entry into research databases, using standardized scales and assessments.
- Participate in data analysis and management, manuscript preparation, and presentation of findings.
- Maintain computerized patient files and databases containing research data generated through protocol studies, performing data searches of medical records for analyses of patient characteristics.
- Support the general implementation, tracking, data acquisition, collection, and reporting of all elements of protocols.
- Manage data through research databases to ensure accurate and reliable data entry.
- Examine and monitor patients during protocol studies, ensuring the collection of a complete clinical database on each patient.
- Provide expertise in clinical trial coordination and management of data acquisition.
- Perform clinical data interpretation and evaluate and interpret protocol and clinical trial findings.
- Document observations and identify and evaluate trends and important findings, communicating information to the multidisciplinary research team for prompt clinical action.
- Monitor activities pertaining to clinical protocols, including patient recruitment and retention, trial progress, and the need for extension or renewal of ongoing trials.
- Present clinical data in terms understandable by patients and other health professionals.
- Develop intake tools and screening forms, working with researchers and medical staff on the general administration of protocols' implementation.
- Collaborate with staff to analyze and evaluate current systems of health care delivery and identify and implement new practice patterns.
Cape Fox Corporation, its subsidiaries, and affiliates provide equal employment opportunities to all persons and prohibit employment decisions based on race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries, and affiliates offer preference to Cape Fox Corporation shareholders, descendants, and other Native Americans pursuant to Public Law 93-638.
