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 ...
This position will act as one of the clinical research coordinators for research projects in the Pulmonary, Critical Care, and Sleep Medicine Division's Clinical Research Unit. The primary responsibilities of this position will involve day-to-day management of clinical trials in areas of data manage...
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...
Must understand and follow good clinical practices for clinical research. The Department of Neurology conducts basic and clinical research on the nervous system and provides clinical care for people with neurological disorders, such as Alzheimer's disease and other forms of dementia, epilepsy, movem...
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...
As a member of the Education Team, the NP Program Clinical Coordinator is primarily accountable to clinical program leadership and faculty of the PMHNP and FNP programs to coordinate the clinical rotations for School of Nursing students. This position serves as a member of the Clinical Education Tea...
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. ...
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 ...
Clinical Research Coordinator Opportunity. Medix is currently seeking experienced Research Professionals wanting to grow their career in the Clinical Research Field. Submits or partners with a regulatory coordinator to submit study related documents, study protocols and study protocol amendments to ...
SF Research Institute is looking for a Clinical Research Coordinator with site experience in San Francisco/Daly City area. Experience with clinical trials within a private research company. ...
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. ...
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...
This is for a phone position, the candidate will need to be able to answer back-to-back phone calls from a shared queue while doing data entry and handling high risk member information, most days are typically call heavy.There will also be entry level intake work done from a fax between calls as ava...
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 ...
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 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...
Coordinates clinical service oversight with CPM and/or Clinical Director. With general supervision, in close coordination with management, develops maintains, monitors and ensures the clinical quality of the assigned component of the program. Leads delivery of clinical services through the developme...
The Clinical Research Coordinator Assistant (CRC-A), in conjunction with Clinical Research Coordinators, assists in the coordination of details of human subjects’ (clinical) research and documentation concerning study protocols. The CRC-A is the entry position in the Clinical Research Coordinator se...
The candidate will assist with clinical evaluations to identify mild cognitive impairment and dementia, will provide specialized research assessments in the context of the ADC multidisciplinary team, will score neuropsychological test results and coordinate submission to data entry, and will assist ...
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...
The primary role of this position is to accurately administer and score standardized neuropsychological test batteries, evaluate cognitive status of potential participants (i.Alzheimers research studies under the supervision of a neuropsychologist and Dr.Meyer at the UC Davis Alzheimers Disease Cent...
Description & Requirements Maximus is hiring a Clinical Review Coordinator - RN/LPN (Remote) to support the Iowa and Connecticut Pre-Admission Screening and Resident Review (PASRR) Programs. The Clinical Operations Mental Health Nurse will prepare detailed summaries of findings by reviewing var...
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...
This position will act as one of the clinical research coordinators for research projects in the Pulmonary, Critical Care, and Sleep Medicine Divisions Clinical Research Unit. The primary responsibilities of this position will involve day-to-day management of clinical trials in areas of data managem...