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UPMCNew
Overview
The Research Associate will execute research protocols for the ECHO Study, including recruiting participants and obtaining informed consent. They will conduct interviews, collect biospecimens, and assist with data cleaning and administrative tasks.
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Compensation
Salary not listed
Posted
New
Mass General Brigham
The coordinator will assist with clinical research studies by recruiting, evaluating, and consenting patients, collecting and organizing patient data, and scheduling study visits. Key duties also involve performing clinical tests like phlebotomy and EKGs, and maintaining study documentation and data integrity.
$20 - $29 / HOUR
3 days ago
American Addiction Centers
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
$31 - $46 / HOUR
Sonic Healthcare USA
The Clinical Research Coordinator is responsible for the identification, retrieval, and processing of archived biological samples for pre-clinical research. They must maintain accurate documentation and ensure all activities comply with federal regulations and IRB guidelines.
5 days ago
Albert Einstein College of Medicine
The technician will manage mouse colonies, including husbandry, genotyping, and compliance with IACUC policies. They will also perform advanced molecular techniques, tissue processing, and assist in neurobehavioral and regenerative medicine research.
$34 / HOUR
7 days ago
Care Access
Support clinical research events by performing phlebotomy, handling biospecimens, and ensuring accurate documentation. Manage event operations including setup, breakdown, and guiding participants through the research flow.
$19 - $44 / HOUR
8 days ago
This event-based role involves supporting participant care and clinical research event operations, including performing venipuncture, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a professional workspace.
$44 / HOUR
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling specimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a safe, compliant workspace.
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling biospecimens, and accurately documenting all procedures according to regulatory standards. Responsibilities also include setting up and managing event stations, ensuring smooth operations, and maintaining compliance and participant safety.
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a safe, professional workspace.
Perform clinical tasks including venipuncture and biospecimen processing to support clinical trials. Handle administrative duties such as participant scheduling, data entry, and maintaining site logs.
$24 - $38 / HOUR
14 days ago
West Virginia University
Independently coordinate and process clinical trial biospecimens for the BioTRAC core, ensuring integrity from collection to shipment. Collaborate with clinical teams and sponsors to maintain protocol compliance and laboratory readiness.
16 days ago
Independently coordinate and process clinical trial biospecimens according to study protocols and regulatory standards. Manage the entire specimen lifecycle from collection and processing to storage and shipment while collaborating with clinical teams.
University of Pennsylvania
Coordinate and implement biomarker-driven clinical trials for thoracic oncology, including patient recruitment and informed consent. Manage study documentation, data entry into REDCap and sponsor databases, and coordinate lab draws and tissue acquisition.
$47,313 / YEAR
The coordinator will assist with the recruitment and maintenance of biospecimen-based GI cancer repositories. Key duties include consenting patients, processing blood and tissue specimens, and managing associated databases and metrics.
Children’s Hospital of Philadelphia
Perform complex immunological assays and high-dimensional spectral flow cytometry on human biospecimens across two research labs. Support multi-omic workflows and contribute to project planning, data analysis, and scientific manuscripts.
$47,020 - $58,780 / YEAR
UVA Health
The Lab Technician is responsible for consenting patients, collecting and processing biospecimens, and managing experimental data logs. They will also coordinate sample distribution and shipping while supporting other lab members with data collection.
$19 - $21 / HOUR
17 days ago
UCSF
The coordinator manages clinical and translational projects, acting as a link between clinicians, research teams, and regulatory authorities. Key duties include overseeing data and specimen management, maintaining regulatory documents, and ensuring IRB compliance.
