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Vitalief
Overview
Support Phase II–III oncology interventional clinical trials by screening, consenting, and enrolling patients. Coordinate care across medical teams and manage study documentation and patient records.
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Compensation
Salary not listed
Posted
21 days ago
City of Hope
The Clinical Research Nurse coordinates oncology clinical trials, managing everything from patient recruitment and informed consent to data collection and biospecimen handling. They ensure strict adherence to federal regulations, study protocols, and institutional SOPs to protect human subjects.
28 days ago
American Oncology Network
Responsible for the clinical and administrative management of complex oncology research studies, including phase 1-3 trials. Key duties include coordinating patient care, ensuring regulatory compliance, and managing study data and budgets.
$26 - $45 / HOUR
1 month ago
Flourish Research
The Clinical Research Coordinator executes Phase I-IV clinical trials by obtaining informed consent and performing protocol procedures. Responsibilities include specimen collection, e-source documentation, and coordinating with study sponsors and CROs.
Coordinates care for patients on clinical research protocols, ensuring compliance with GCP and FDA guidelines. Manages study procedures, regulatory documentation, and the administration of investigational products.
$25 - $46 / HOUR
Sanford Health
This role involves learning daily clinical trial management procedures by assisting in the planning, designing, coordinating, and implementation of research studies or projects. The coordinator will also provide interpretation and coordination of services for patients and facilitate necessary communication.
$21 - $33 / HOUR
Medpace, Inc.
The Study Start-Up Coordinator communicates with research sites to collect essential documents for clinical trials and maintains quality reviews of trial documents. They also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality review of trial documents. They will also manage timelines for study start-up through collaboration with internal teams.
The Project Coordinator will engage in clinical trial management and work closely with the project CTM to ensure timely delivery of tasks. Responsibilities also include compiling project status reports, interacting with sponsors and study sites, and managing study supplies.
2 months ago
The role involves engaging in day-to-day clinical trial management, working closely with the CTM to ensure timely and accurate task delivery. Responsibilities also include compiling status reports, interacting with various stakeholders, and managing internal regulatory filing oversight and study supplies.
US Foot & Ankle Specialists
The Clinical Research Coordinator manages and conducts clinical research projects by leading trial operations, ensuring adherence to Standard Operating Procedures (SOPs), and acting as a liaison between investigators, sponsors, and regulatory bodies. Key duties include monitoring study activities, maintaining detailed records, managing subject enrollment, and handling adverse event reporting.
4 months ago
