This position provides coordinator support of research trials and related studies in theUC Davis Transplant Center. Industry-sponsored, grant-sponsored, registries, andinvestigator-initiated studies are conducted in the field of transplantation.
The assistant clinical research coordinator (CRC) is responsible for assisting more senior staff with several aspects of the conduct of clinical trials, including (but not limited to) : subject recruitment, screening, enrollment, scheduling, physical performance testing, data collection, participant tracking, preparation for audits and monitor visits, study closeouts, and assisting with administrative requirements.
Additional responsibilities include (but are not limited to) assisting with : IRB submissions, modifications, amendments, annual renewals, obtaining financial disclosure information from the investigators, and collection and maintenance of study regulatory documents.
Work is performed under consultative direction of the Principal Inves
Clinical Research Coordinator II - Pediatric Neonatology - Full-Time, Hybrid
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator II - Pediatric...
Clinical Research Coordinator II - Pediatric Neonatology - Full-Time, Hybrid
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator II - Pediatric...
Clinical Research Coordinator II (Oncology)
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
Clinical Research Coordinator I - Obstetrics & Gynecology - Maternal-Fetal Medicine (Part-Time, Hybrid)
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I - Obstetrics & Gynecol...
Clinical Research Assistant- 233673
The Clinical Research Assistant will support the clinical research team in conducting clinical trials and studies in accordance with regulatory guidelines. Coordinate with clinical staff, physicians, and research coordinators to ensure smooth trial operations. Maintain accurate and detailed records ...
Clinical Research Coordinator I - Kerlan Jobe Institute
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Clinical Research Coordinator
Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Assist with ma...
Clinical Research Coordinator I - Medicine/Endocrinology
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Maintains research practices usi...
Clinical Research Coordinator I - Kerlan Jobe Institute
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I - Kerlan Jobe Institut...
Clinical Research Coordinator
This is a clinical research position partially funded by a Shriners Hospitals Clinical Outcomes Studies research grant. Position responsibilities include: provide support and ensure site compliance with the Grant Proposal; assemble / process / coordinate approval for The Home Office and local Human ...