The Clinical Research Budget Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time, ...
As a Clinical Research Coordinator III, 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 ...
As a Study Coordinator in clinical research, you will be responsible for human subject recruitment, screening, enrollment, and retention. Five or more years of experience as a study coordinator for clinical research. Play a key role with a world-renowned leader in medical research. Data management e...
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. Responsible for compiling and reporting on e...
Seeking dynamic Research Coordinator to coordinate complex research projects, including developing study protocols, managing logistics, and handling regulatory tasks. The vital importance of epidemiologic research was highlighted by the COVID-19 pandemic, in which epidemiologists have helped to trac...
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 ...
Training Coordinator (Clinical Research) - (Glendale, California, United States). Training Coordinator is a business-critical role to ensure that clinical trials are conducted according to local regulations, international guidelines, SOPs, and protocols by coordinating and performing, where appropri...
Under the general direction from the Vice Chair for Research, the Research Operations Coordinator (ROC) will provide administrative support to the basic science, translational and clinical research missions of the Department of Anesthesiology & Perioperative Medicine (DAPM). The Research Operati...
The Research Administrative Coordinator plays a critical role in supporting the research operations of the Heart Institute. Job Title: Research Administrative Coordinator. The Smidt Heart Institute at Cedars-Sinai Medical Center is a world-renowned leader in heart disease research and treatment. Thi...
Prepare and process all Institutional Review Board (IRB)through the IRB and other regulatory groups as apropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events.Coordinate, organize and maintain all documentation required by sponsor or CRO (c...
Req ID : 1696 Working Title : Clinical Research Coordinator I - Alzheimer's and Dementia Research Program - Department of Neurology (Hybrid) Department : Research - Neurology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial...
The Research Nurse Coordinator II is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical l...
As a Clinical Research Data Coordinator, you will play an indispensable role in the success of our clinical research projects. A Private Practice in West Los Angeles that specializes in Oncology is searching for a highly motivated and detail-oriented Clinical Research Data Coordinator to join their ...
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. Work alongside physician-scienti...
Overview Purpose Statement/Position Summary: The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Certi...
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 ...
A Higher Education institution is looking for a Clinical Research Coordinator to support their team in Westwood CA. The Clinical Research Coordinator will support teams with all aspects of study coordination, including recruiting, scheduling patient visits, assessing patients, taking notes, followin...
Req ID : 3048 Working Title : Clinical Research Coordinator I - Pituitary Center Department : Research Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift Duratio...
Establish and maintain relationships with targeted organizations and utilize those relationships to strategically implement the continued care model, placing patients into longitudinal treatment within the community.Maintain a vast understanding of multiple pathways to wellness including harm reduct...
Responsible for all aspects of clinical research from initiation through completion of research projects with human subjects. One year of research experience. Demonstrated track record of human subjects research coordination, informed consent procedures and documents. Has knowledge in human subjects...
Prior experience as a Clinical Research Coordinator at a research site. Job Title: Clinical Research Coordinator. Experience as a coordinator for HIV clinical trials is preferred, but not required. Working experience of the start-up and closure of clinical research studies and patient registration a...
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 ...
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research...
Overview Purpose Statement/Position Summary: The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Certi...
Prior experience as a Clinical Research Coordinator at a research site. Position: Clinical Research Coordinator. Job Title: Clinical Research Coordinator. Experience as a coordinator for HIV clinical trials is preferred, but not required. ...