Registered Nurse

2 weeks ago

Bethesda, United States Akahi Associates, LLC Full time

Overview:
**Job title**:Research Nurse

**Overall Position Summary and Objectives**:
To provide services and deliverables through performance of support

services.

**Min Education**:
Associate's

**Schedule**:
Monday - Friday, regular office hours. No nights.

**Benefits**:
PTO, 11 paid Government Holidays, sick leave, health insurance, vision insurance, dental insurance

**Statement of Work Details**
- Recruits and screens patients for inclusion in protocols and clinical trials
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.
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
- Performs assessments and physicals, and collects medical histories
- 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.
- Administers protocol consents and documentation and monitors compliance.
the potential risks.
- Collaborate with researchers and medical staff to obtain and maintain informed consent and assent and address
ethical and legal implication 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 variance 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
- Performs data input and management
- 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 professional 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

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