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M3USA
Overview
The coordinator supports site-based trial execution by ensuring compliance with regulatory standards and managing study documentation. Key duties include performing delegated clinical procedures, conducting informed consent, and coordinating participant visits.
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Compensation
Salary not listed
Posted
21 days ago
Rovia Clinical Research
Coordinate and execute clinical trials by conducting patient visits and performing clinical tasks like phlebotomy and ECGs. Ensure data integrity through accurate source documentation and EDC entry while maintaining protocol adherence.
$20 - $24 / HOUR
22 days ago
St. Luke's University Health Network
The coordinator is responsible for the screening, enrollment, and coordination of clinical trials while ensuring compliance with protocol and federal regulations. Key duties include managing study documentation, performing study procedures, and coordinating data collection across departments.
24 days ago
Olema Oncology
Provide administrative and operational support to clinical teams for in-house and outsourced trials. Manage study documentation, vendor relationships, and investigator site communications to ensure trial execution.
$110,000 - $120,000 / YEAR
27 days ago
Nationwide Children's Hospital
Manages clinical study elements including recruitment, enrollment, and day-to-day management following ICH/GCP guidelines. Responsible for collecting research data, processing human specimens, and maintaining regulatory binders.
29 days ago
1 month ago
Theradex Oncology
The Clinical Research Associate will conduct site monitoring visits, including qualification, initiation, routine, and close-out visits to ensure protocol compliance and data integrity. They will also act as a liaison between study sites and the project team while managing site documentation and safety reporting.
$75,000 - $145,000 / YEAR
The coordinator manages ophthalmology clinical trials by executing study protocols and performing specialized eye exams. They are responsible for patient enrollment, data integrity in EDC systems, and ensuring compliance with ICH/GCP guidelines.
$55,000 - $65,000 / YEAR
The Clinical Research Coordinator coordinates and executes clinical trials by managing patient visits and ensuring adherence to study protocols and GCP guidelines. Key duties include performing clinical tasks, managing data entry in EDC systems, and maintaining investigational product accountability.
$50,000 - $55,000 / YEAR
University of Colorado
This position manages clinical trial treatment plans and ensures adherence to FDA, NCI, and institutional regulatory standards. The role involves collaborating with research teams to document clinical procedures and performing informatics support to improve research workflows.
$40,762 - $51,849 / YEAR
This position is responsible for conducting key aspects of Phase I-IV clinical trials in accordance with FDA regulations and institutional standards. The role involves managing treatment plans, performing clinical research informatics, and collaborating with multidisciplinary teams to ensure effective study documentation.
Bon Secours Health System
Coordinates clinical research projects by recruiting study participants, ensuring protocol compliance, and managing research materials. Acts as a liaison between investigators, patients, and regulatory bodies while performing clinical procedures and data management.
IQVIA
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
$71,900 - $145,300 / YEAR
2 months ago
UCSF
The Clinical Research Coordinator will support and coordinate clinical and translational research projects within the Division of Cardiology. Responsibilities include managing study operations, ensuring compliance with research protocols, and facilitating communication between stakeholders.
$38 - $61 / HOUR
This role involves managing the day-to-day operations of clinical studies, ensuring execution aligns with protocols, GCP, and SOPs, including coordinating startup activities, overseeing facility issues, and leading site meetings. Responsibilities also include monitoring enrollment progress, ensuring timely data entry into platforms like EDC, leading study visits, and providing guidance and training to site research staff.
$55,000 - $70,000 / YEAR
3 months ago
