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Orlando HealthNew
Overview
Develop, coordinate, and implement research and administrative strategies for the management of clinical trials. Support the execution of research studies to provide patients with innovative diagnosis and treatment options.
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Compensation
Salary not listed
Posted
New
Mass General BrighamNew
Provides assistance on clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. Performs clinical tests such as phlebotomy and EKGs and maintains regulatory binders and documentation.
$21 - $29 / HOUR
Beth Israel Lahey HealthNew
The Clinical Research Coordinator I manages the administration of multiple research studies, ensuring protocol adherence and regulatory compliance. Key duties include recruiting and screening participants, collecting study data, and maintaining professional relationships with sponsors and CROs.
$22 - $27 / HOUR
Children's Hospital of PhiladelphiaNew
The role involves the complete coordination of clinical research activities, including patient recruitment, informed consent, and adherence to IRB protocols. Responsibilities also include managing regulatory documents, collecting laboratory specimens, and ensuring GCP compliance.
$56,890 - $71,110 / YEAR
Cooper University HospitalNew
Assists the Principal Investigator with IRB protocols, consent forms, and study budget development. Manages study documentation, research billing in EPIC, and the recruitment of study participants.
$29 - $48 / HOUR
University of Massachusetts Medical School
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
4 days ago
University of Louisville
Coordinates daily activities for oncology clinical trials, including patient screening, data collection, and specimen processing. Acts as a liaison between participants and the clinic while maintaining research records and regulatory reports.
$21 - $32 / HOUR
University of Florida
Coordinates clinical research protocols by recruiting participants, managing informed consent, and ensuring regulatory compliance. Acts as a liaison between investigators, sponsors, and IRBs while managing study documentation and finances.
$53,000 - $57,000 / YEAR
The Clinical Research Coordinator II will coordinate regulatory activities and manage data collection for complex research protocols. They will also ensure compliance with study protocols and assist with participant interactions and documentation.
$48,000 - $55,000
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling visits, and ensuring compliance with study protocols.
$40,000 - $48,000 / YEAR
ObjectiveHealth
The coordinator is responsible for managing assigned clinical studies, including patient identification, screening, enrollment, and conducting clinic visits. They must ensure strict protocol adherence and maintain clean data entry and regulatory compliance.
Coordinate clinical research trials by managing patient identification, screening, enrollment, and conducting clinic visits. Perform direct patient care activities including blood draws, ECGs, and maintaining strict protocol adherence and regulatory compliance.
The US Oncology Network
The role is responsible for recruiting, screening, and enrolling patients in clinical trials while ensuring strict protocol compliance. It involves coordinating participant visits, documenting assessments, and maintaining regulatory documents in accordance with GCP and SOPs.
Johnson County Clintrials LLC
The Clinical Research Coordinator II manages multiple concurrent clinical trials, serving as the primary liaison between sponsors, investigators, and clinical staff. Key duties include subject screening, protocol adherence, regulatory documentation, and performing clinical procedures to ensure study integrity.
The Clinical Research Coordinator II manages multiple concurrent clinical trials, serving as the primary liaison between sponsors, investigators, and clinical staff. Key duties include subject eligibility assessment, protocol adherence, and maintaining rigorous regulatory documentation.
Headlands Research
Manage and execute Phase I-IV clinical studies from site initiation to close-out in compliance with FDA and GCP guidelines. Coordinate subject visits, maintain accurate documentation, and collaborate with investigators and sponsors.
The coordinator is responsible for managing human subject research tasks, including obtaining participant consent and maintaining regulatory documentation. They also handle data collection, monitor protocol compliance, and assist with grant and manuscript preparation.
The coordinator is responsible for managing human subject research tasks, including obtaining participant consent and maintaining regulatory documentation. They also handle data collection, study visit scheduling, and ensure strict adherence to IRB and GCP guidelines.
Mount Sinai Health System
The coordinator assists in daily clinical research activities, including obtaining informed consent and organizing study information. They also help prepare grant applications and documents for the Institutional Review Board and Grants and Contracts Office.
$58,661 - $73,530 / YEAR
5 days ago
Memorial Healthcare
Coordinates the implementation of multiple clinical research studies, including managing IRB submissions and regulatory compliance. Responsible for training staff, handling adverse events, and conducting sponsor visits.
