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CenExelNew
Overview
The Patient Care Technician I provides psychosocial support and advocacy for psychiatric patients participating in clinical trials. Responsibilities include assisting with activities of daily living, coordinating discharge planning, and ensuring adherence to clinical protocols and FDA regulations.
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Compensation
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Posted
New
Evolution Research Group
The Unit Clinician supports clinical trials by dispensing investigational drugs and collecting biological samples according to physician orders. They are responsible for performing ECGs, venipuncture, and ensuring strict adherence to Good Clinical Practices (GCP).
$24 - $28 / HOUR
3 days ago
The Unit Clinician supports clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing ECGs, venipuncture, and ensuring all procedures follow Good Clinical Practices and doctor's orders.
$18 - $22 / HOUR
Nevada System of Higher Education
The Clinical Research RN manages oncology research projects, including participant recruitment, consenting, and clinical monitoring. They coordinate with investigators to implement protocols, manage study databases, and ensure accurate data collection and reporting.
$38 - $59 / HOUR
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.
5 days ago
This role involves primary and back-up coordination of multiple studies with minimal supervision, ensuring strict adherence to study protocols and meeting all deadlines. The coordinator will also perform literature reviews, assist with manuscript writing, and train junior staff members on compliance with regulatory guidelines.
$25 - $37 / HOUR
Provide direct nursing care and administer investigational treatments for Phase I-IV clinical trials. Collaborate with medical staff to ensure participant safety and strict adherence to research protocols.
6 days ago
Dartmouth-Hitchcock Health
Supports basic administrative clinical trial tasks including subject management, data entry in CTMS, and maintaining regulatory records. Assists with IRB submissions and ensures compliance with GCP guidelines and institutional processes.
University of Pennsylvania
The role involves coordinating complex oncology clinical trials, ensuring protocol execution according to GCP and HIPAA standards. Responsibilities include managing patient visits, handling regulatory submissions, and maintaining audit-ready study files.
$53,418 - $60,813 / YEAR
11 days ago
Georgetown University
Manage and coordinate a subset of clinical trials focusing on neuroimmunology and neuromuscular diseases, ensuring strict protocol adherence during patient visits. Responsible for regulatory maintenance, accurate data entry in OnCore/CTMS, and maintaining constant communication with patients and sponsors.
$44,022 - $73,407 / YEAR
16 days ago
Benaroya Research Institute
Provide administrative and operational support for cancer clinical trials, including regulatory maintenance and participant scheduling. Perform clinical procedures such as blood draws and vitals while managing study databases and supplies.
$24 - $34 / HOUR
17 days ago
Cleveland Clinic
Coordinate the implementation of human subject research projects while providing comprehensive nursing care to adult and pediatric patients. Responsibilities include administering study treatments, collecting clinical data, and ensuring adherence to research protocols and regulatory standards.
18 days ago
Washington University in St. Louis
This role coordinates and implements research studies, managing data collection while ensuring continuity of patient care and protection of human subjects under the Principal Investigator's guidance. Responsibilities include providing direct patient care, administering study interventions and medications, processing specimens, and collaborating with multidisciplinary teams and sponsors.
$56,200 - $96,100 / YEAR
1 month ago
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.
CenExel
This role involves advocating for research participants by addressing their psychosocial needs and assisting with retention during clinical trials, which includes performing phlebotomy and managing case needs.
$18 - $19 / HOUR
4 months ago
