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 ...
Society for Clinical Research Associates (SOCRA) Certified Clinical Research Professional (CCRP) or Association of Clinical Research Professional (ACRP) Certified Clinical Research Coordinator (CCRC). Clinical Research Coordinators (CRCs) provide support, coordination, and leadership for investigato...
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...
The main function of a Clinical Support Coordinator is to serve as initial point of contact for providers and members in medical management. ...
The Clinical Research Coordinator must also be able to perform clinical. Writes patient information sheet for clinical studies for submission to IRB, as well as. Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as. ...
Prior experience as a Clinical Research Coordinator at a research site. Experience as a coordinator for HIV clinical trials is preferred, but not required. Working knowledge and previous experience with clinical trials, data management and case report forms. Working experience of the start-up and cl...
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...
While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical ...
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...
We have an opportunity for a Nurse Clinical Coordinator in our Surgical Services department. ...
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 are seeking a dedicated Clinical Research Coordinator to join our team. The individual will be responsible for managing and coordinating clinical trials and research studies in compliance with regulatory guidelines and protocols. This role involves working closely with principal investigators, re...
ABA Clinical Coordinator (Program Supervisor). Provide clinical training and support to a dedicated team. ...
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...
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. Our team of scientists develop s...
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. ...
The main function of a Clinical Support Coordinator is to serve as initial point of contact for providers and members in medical management. ...
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...
Program Services Clinical Coordinator Everybody needs a job but only extraordinary people work here. ...
The Specialty Resource Coordinator - RN is responsible for coordinating assigned surgical specialty services within the Main OR and in the Procedure Center; to function as an expert practitioner (circulator role) whose intuition and skill arise from comprehensive knowledge thoroughly grounded in exp...
DaVita is seeking a Clinical Coordinator who is looking to give life in a hospital setting. In this vital Registered Nurse role, you will have the opportunity to excel as the superior dialysis nurse, mentor and clinical expert you are-and have a dramatic impact on the lives of our patients and their...
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. Works closely with a regulatory coordinator ...
Ensure you and your clinical team are delivering the highest level of care to our patients by ensuring their safety, comfort, and well-being. Dialysis Charge RN readiness approval by Clinical Nurse Manager or RN-licensed FA/GFA required. DaVita is a clinical leader! We have the highest percentage of...
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...
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...