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Cleveland Clinic
Overview
Coordinate the implementation and conduct of human subject research projects, including complex trials and regulatory documentation. Serve as a liaison between investigators and research personnel while ensuring protocol compliance and effective data management.
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Compensation
Salary not listed
Posted
2 days ago
University of Iowa
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
3 days ago
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
8 days ago
The Research Nurse Coordinator oversees the implementation and conduct of human subject research projects while ensuring adherence to protocols. They perform nursing assessments, manage regulatory documentation, and serve as a liaison between the research team and study participants.
Evolution Research Group
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
9 days ago
Mercyhealth Wisconsin and Illinois
The Clinical Research Coordinator is responsible for recruiting and consenting study participants, managing regulatory documentation, and ensuring protocol adherence. They also handle specimen collection and processing while maintaining accurate data submission and reporting adverse events.
$27 - $42 / HOUR
ICON plc
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with site staff and investigators to facilitate study conduct and prepare essential study documentation.
17 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
University of Massachusetts Medical School
The Clinical Research Coordinator manages human subject research protocols, including regulatory documentation, participant visits, and data collection. They ensure compliance with federal and institutional guidelines while supporting investigators with grant preparation and study reporting.
21 days ago
The Research Nurse Coordinator I manages complex research protocols, ensuring adherence to GCP standards and regulatory requirements. They act as a primary liaison between clinical partners, investigators, and sponsors while overseeing patient care and data integrity.
The Clinical Research Coordinator I manages regulatory activities, participant visits, and data collection for research protocols. They ensure compliance with IRB, HIPAA, and Good Clinical Practice guidelines while supporting the Principal Investigator.
23 days ago
UT Health San Antonio
Responsible for assisting with the administration, organization, and implementation of clinical trial operations and systems management. Provides technical reviews of research protocols, funding agreements, and billing processes.
Oregon Health & Science University
The Senior Clinical Research Assistant manages patients on clinical trials, including consenting, enrolling, and gathering data. They are also responsible for regulatory tasks, sample processing, and assisting the Clinical Research Manager with various projects.
$48,734 - $77,522 / YEAR
The coordinator is responsible for managing human subject research, including regulatory activities, data collection, and participant coordination. Duties range from obtaining consent and tracking milestones to supervising staff and ensuring protocol compliance across multiple levels of seniority.
$40,000 - $80,000 / YEAR
24 days ago
Neurocrine Biosciences
Supports Clinical Operations by managing the quality, compliance, and inspection-readiness of Trial Master Files (TMF). Acts as a subject matter expert for eTMF systems, facilitating audits and collaborating with cross-functional teams to maintain study documentation.
$89,800 - $123,000 / YEAR
UCSF
Execute and coordinate clinical research protocols, including data collection and the management of human biospecimens. Manage regulatory documents, IRB submissions, and ensure compliance with institutional and agency policies.
$32 / HOUR
25 days ago
ALX Oncology Inc.
Supports clinical operations by managing the Trial Master File (TMF), coordinating site activation, and tracking study documents. Collaborates with CROs and internal teams to ensure regulatory compliance and efficient trial execution.
$100,000 - $120,000 / YEAR
29 days ago
Structure Therapeutics
The Senior Clinical Trial Associate supports the planning and implementation of clinical studies by managing study-related documents and the Trial Master File. They act as a central contact for study teams, coordinating with vendors, investigative sites, and cross-functional groups.
$110,000 - $120,000 / YEAR
1 month ago
University of Rochester
Coordinates administrative and clinical activities for human subject research projects focusing on muscular dystrophy. Responsibilities include participant recruitment, regulatory document management, and overseeing data integrity for clinical trials.
$21 - $30 / HOUR
Carilion Clinic
The coordinator assists with administrative activities for industry, grant, or internally funded research studies while ensuring compliance with institutional and governing policies. Key duties include recruiting participants, obtaining informed consent, collecting data, and managing regulatory documentation for the IRB and FDA.
