Research Nurse.

Concentric Methods is seeking a Research Nurse to join our team in Bethesda, MD in support of the NIH.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 such as laboratory test results and socialbackground.Interview patients to obtain medical history, sexual history, medication history, history of use of substances such as alcohol and recreational drugs, previous HIV-related risks factors, and history of participation in other clinical research.Assist research and medical staff interview, screen, and evaluate the appropriateness of eligible subjects for participation in the research protocol.Participate in recruitment and outreach activities and contribute to recruitment strategies through innovative ideas.Recruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol.Design and maintain a selection of materials appropriate to send to health care referral sources seeking eligibility information or 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 of subjects on aspects of subject's care, treatments, and side effects.Provide information about the study to referring physicians, advocacy groups, NIH offices, and in response to inquiries from potential study participants.Participate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research.Obtain and record complete health histories and conduct physical assessments; communicate data from these and other sources.Manage clinical and research support activities to ensure patient safety and address the clinical needs of the patients.Review findings from assessments and other sources in clinical rounds.Review charts to collect relevant clinical data such as laboratory test results and social background.Complete medical and psychiatric assessments of potential participants in multiple research protocols by collecting and reviewing past and present medical records and conduct interviews with research applicants and their families.Conduct family interviews to obtain comprehensive understanding of the care needs of the patient.Continually assess ongoing understanding of the research process for patients and families and provide teaching and support as indicated.Ensure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks.Collaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implications of the research protocol.Contribute to all study-related IRB and regulatory matters, including all reporting requirements (including deviations, unanticipated problems, adverse events), and report issues and variances promptly to the research team.Collect and report data to appropriate regulatory and monitoring agencies.Perform quality assurance and quality control activities relating to protocol adherence, protocol monitoring, data collection, data abstraction and data analysis and protect research participant data in accordance with regulatory requirements.Perform accurate data entry into research database, including the use of standardized scales and assessments.Participate in data analysis and management as well as manuscript preparation and presentation of findings.Maintain computerized patient files and databases containing research data generated through protocol studies and perform data searches of medical records for analyses of patient characteristics.Support the general implementation, tracking, data acquisition, collection, and reporting of all elements of the protocols.Manage data through research databases to ensure accurate and reliable data entry.Examine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient.Provide expertise in clinical trial coordination and management of data acquisition.Performs clinical data interpretation and evaluates and interprets 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 such as monitoring patient recruitment and retention, trial progress, and the need for extension or renewal of ongoing trials.Present clinical data in terms which may be understood by the patient, as well as interpretation at a level which is conversant with other health professionals including physicians.Develop intake tools and screening forms and work 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 to identify and implement new practice patterns.

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