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Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
EPO
Scheduled Hours 40 Position Summary Position assists investigators as a data coordinator of clinical research trials of all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it into an Electronic Data Capture (EDC).May
Kumc
Department: SOM KC Internal Medicine - Gastroenterology and Hepatology ----- Medicine-Gastroenterology Position Title: Clinical Research Coordinator - Internal Medicine (Gastroenterology) Job Family Group: Professional Staff Job Description Summary: The Clinical Research Coordin
University of Arizona Comprehensive Cancer Center
Participant Coordination, Visit Execution, and Basic Clinical Support: Following detailed instruction, will recruit, screen, consent, and schedule study participants. With instruction, prepare visit materials and assist with visit flow for physical assessments (e.g., 6MWT, active
Mount Sinai Health System
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects
Mount Sinai Health System
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects
Mount Sinai Health System
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects
University of Arizona Police Department
Participant Coordination, Visit Execution, and Basic Clinical Support: Following detailed instruction, will recruit, screen, consent, and schedule study participants. With instruction, prepare visit materials and assist with visit flow for physical assessments (e.g., 6MWT, active
Allegheny Health Network
Company : Allegheny Health Network Job Description : GENERAL OVERVIEW: This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources. Maintai
University of Virginia
The Department of Pediatrics in the University of Virginia’s (UVA) School of Medicine is seeking candidates for a Clinical Research Coordinator (CRC), licensed or non-licensed, at experience levels CRC 2 through CRC 4. The CRC will support clinical research efforts for the Pediat
University of Virginia
The Department of Pediatrics in the University of Virginia’s (UVA) School of Medicine is seeking an applicant for a Clinical Research Coordinator (CRC), Level 1 (wage) to join the NICU/PICU CRC team in supporting Neonatal Intensive Care Unit (NICU) research. This CRC-1 will play
Mount Sinai Health System
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects
Mount Sinai Health System
The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time employees.
Mount Sinai Health System
The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time employees.
Tekton Research
Responsible for the daily operations and overall management of assigned clinical trials including administrative duties and regulatory functions. Responsible for clear and direct communication with study sponsor, study monitor, CRO, PI and site management. Adherence to Tekton SOP
Tekton Research
Team Tekton is now hiring a Clinical Research Coordinator I in Fort Collins, CO . Responsible for the overall management the studies assigned to you including administrative duties, such as regulatory functions. Responsible for clear and direct communication with study sponsor, s
Tekton Research
The CRC II is r esponsible for the daily operations and overall management of assigned clinical trials including administrative duties and regulatory functions. Responsible for clear and direct communication with study sponsor, study monitor, CRO, PI and site management. Adherenc
CenExel
Independently responsible for coordinating all aspects of multiple and/or complex clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
CenExel
Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Dana-Farber Cancer Institute
This Satellite Clinical Research Coordinator position will work within the Dana-Farber Attleboro Satellite location supporting the clinical research program and research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Princip
Biological Sciences Division at the University of Chicago
Department BSD PED - Clinical Trials Office About the Department In the Department of Pediatrics at the University of Chicago, we strive to provide the highest level of complex care for children from diagnosis and treatment to conducting research to find promising new therapies
Osu
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Profound Research
About Profound Research Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model
Jeffersonhealth
Job Details Supports innovative, patient-centered research in population science and cancer control, focused on improving the experiences and outcomes of individuals with cancer and their family caregivers. The research program integrates qualitative and quantitative methodologie
Mount Sinai Health System
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and C
University Health KC
If you are a current University Health or University Health Physicians employee and wish to be considered, you must apply via the internal career site. Please log into myWORKDAY to search for positions and apply. Clinical Research Coordinator - Women's Health Department 10