Clinical Research Nurse Chenega · Bethesda, MD Posted yesterday

# Clinical Research Nurse Chenega
· Bethesda, MDTailor My Resume Start free. No credit card.### About the role

Summary

Chenega Services and Federal Solutions (CSFS) is seeking a Research Nurse to provide support services to the National Institutes of Health (NIH) Clinical Center.

Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, innovative solutions for our clients.### Responsibilities
* Ensures human subjects protections and patient-orientation during the course of a research subject’s participation in clinical research protocol.
* Assists with protocol development, implementation, and management including overseeing the collection of concise and verifiable data that contributes to public health.
* Performs duties in the following areas: protocol compliance, contributing as a co-investigator on clinical trials as well as various collaborative projects, adherence to ethical standards, informed consent, patient recruitment and retention, management of clinical trials patients, documentation and document management, data management and information technology, financial stewardship, and leadership and professional development.
* Assists in developing clinical research and protocol-specific standards of practice (SOP).
* Develops, implements, and assesses process improvement strategies for compliance with applicable regulations and SOPs.
* Develops and institutes a nursing feasibility review process to assess the ability to implement the protocol trial within local nursing care practices and standards.
* Develops methods to overcome institutional and external barriers to protocol compliance.
* Collaborates with the principal investigator to finalize, ensure implementation, assess efficacy, and revise corrective and preventive action plans.
* Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.
* Collaborates with PIs to resolve protocol implementation problems during design period; uses and revises/creates data capture forms to meet study needs.
* Directs the activities of multiple personnel involved in trials through clear delineation of responsibilities, endpoints, and approaches based on scope of practice and/or training.
* Assures compliance of clinical trial objectives and endpoints.
* Collaborates with health care members in the execution and management of trials; communicates findings and suggestions to the PI based on expertise; reports clinical data to regulatory and monitoring agencies; produces reports for clinical use and treatment decision-making; and summarizes clinical data as requested by PIs.