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 appropriate, awareness, orientation, and skills training for all staff. Highly preferred 1...
A company is looking for a Clinical Research Finance Coordinator II (Pre-Award) to manage financial aspects of clinical research studies during the pre-award phase. ...
As a Clinical Research Coordinator, you will execute and coordinate a variety of specialized clinical research activities within the Early Phase Clinical Unit (EPCU), ensuring that assigned protocols are executed with high quality, and Standard Operating Procedures (SOPs)and GCP/ICH guidelines are f...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, communicating non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each stu...
The Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years: Experience in a Clinical Research setting. ...
DescriptionThe Department of OBGYN is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. Mathematical skills sufficient to prepare clinical resea...
Cedars-Sinai is seeking a Clinical Research Finance Coordinator II (Pre-Award) to join our dynamic research team. The Clinical Research Budget Coordinator II develops complex clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evalu...
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 Finance 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,...
The ADRC is an interdisciplinary group of researchers including faculty investigators, research coordinators, health professionals, and trainees who are committed to research on memory problems and aging. The ADRC Research Coordinator will work with USC investigators and research staff to coordinate...
The Fuller Youth Institute (FYI) at Fuller Theological Seminary seeks a Research Project Coordinator to support and help implement research activities. Assist in coordinating high-quality research that takes into account the diversity of the population's values, beliefs, and behaviors when developin...
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...
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...
Cedars-Sinai is seeking a Clinical Research Finance Coordinator II (Post-Award) to manage the financial operations of clinical research projects after award funding has been secured. The Clinical Research Finance/Budget Coordinator II develops complex clinical trial budgets for industry, National In...
Job Description The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Jobs-Indeed R...
The Clinical Research Coordinator III 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 oversight of all studies wi...
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...
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...
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...
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...
Req ID : HRC1394612 Working Title : Clinical Research Coordinator I - Smidt Heart Institute Department : Heart Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift...
Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry.Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.Assure compliance with the protocol and regulatory requirements includes: collecting, recording...
Are you ready to continue your career journey with us!? The Research Administrative Coordinator works under the direction of the Research Director, Research Manager, and the Research Operations Associate of the assigned research area. Req ID : 2199 Working Title : Research Administrative Coordinator...
We’re seeking a self-motivated, independent professional with: * Knowledge of health services or clinical research methodology and principles * Computer proficiency with Microsoft Word/Excel/Publisher/Access * In-depth understanding of Human Subject Protection and informed consent * Experience follo...
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 experience of the start-up and closure of clinical research studies and patient registration and randomization. ...