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. Clinical Research Coordinator I ...
Under the direction of the study site PIs and supervised by the Clinical Research Supervisor, this position serves as Senior Clinical Research Coordinator for the Department of Public Health Sciences. The incumbent will provide leadership for the clinical research program, including guiding and ment...
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...
Assistant Clinical Research Coordinator. The Assistant Clinical Research Coordinator will initiate, conduct, and publish research studies connected to nutrition as it relates to muscle biology and metabolic health. Relevant skills include experience performing tissue culture, writing and working clo...
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...
This is a clinical research position partially funded by a Shriners Hospitals Clinical Outcomes Studies research grant. This position's primary function is to serve as a Coordinator for the grant(s) funding the position. Position responsibilities include: provide support and ensure site compliance w...
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...
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. Perform clinic...
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...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
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. Clinical Research Coordinator I ...
We are looking for a Clinical Transition Coordinator to join our Northern CA team!. We’re expanding our team and seeking a passionate and dedicated Clinical Transition Coordinator to make a significant impact in our patients' lives. Are you a compassionate healthcare professional with a knack for co...
We have an opportunity for a Nurse Clinical Coordinator in our Surgical Services department. The Clinical Coordinates and supervises the care of patients and collaborates with other members of the health care team to plan, implement, and evaluate appropriate interventions. ...
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...
Description & Requirements Maximus is hiring a Clinical Review Coordinator - RN/LPN (Remote) to support the IN LCAR program. The Clinical Review Coordinator Nurse will review summaries of findings by reviewing various information sources to identify service needs related to the individual's men...
Are you ready to bring your clinical skills to a world-class facility recognized as top ten in the United States for transplant services? Do you have a passion for the highest quality and patient satisfaction? Then please respond to this dynamic opportunity available with one of the best places to w...
Our approach involves human physiology and multi-center longitudinal cohort studies, case-control studies, and clinical trials. ...
The Clinical Services Coordinator, Intermediate (CSC) will report directly to the supervisor of care management support operations and will serve as initial point of contact for providers and members in the medical management process by telephone or correspondence. ...
Assistant Clinical Research CoordinatorUnder direction of the Principal Investigator supporting the Baar Lab for the Periodic Table of Food Initiative- Phase II Studies- Precision Protein-Based Food Products for an Equitable, Sustainable, and Healthy Global Population Project. The Assistant Clinical...
The Clinical Services Coordinator Intermediate will report to the CHP Manager. The Children’s Health Program (CHP) team provides identification, referrals, and care management for all Medi-Cal members under years old and collaborates within Promise Clinical Team. In this role you will work with cli...
ABA Clinical Coordinator (Program Supervisor). Provide clinical training and support to a dedicated team. ...
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. Works closely with a regulatory coordinator or directl...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
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. Works closely with a regulatory coordinator or directl...