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University Retina
Overview
The Clinical Research Assistant is responsible for recruiting and screening subjects and coordinating patient visits for clinical trials. They must collect accurate research data and ensure strict adherence to study protocols and GCP guidelines.
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Compensation
$21 - $24 / HOUR
Posted
2 days ago
Houston Retina Associates
Akido
Manage the end-to-end credentialing and enrollment process for providers with health plans, Medicare, Medicaid, and hospitals. Maintain accurate provider data in MD Staff and resolve complex enrollment issues to ensure uninterrupted patient care.
$24 - $33 / HOUR
Ember Health
Administer IV ketamine treatments and monitor patients to ensure safety and comfort. Manage medical inventory and maintain clean clinical spaces while building trusting relationships with patients.
$93,000 / YEAR
Children’s National Hospital
The Clinical Research Assistant supports clinical research by identifying eligible participants and conducting protocol-specific testing and interviews. They are responsible for maintaining accurate study documentation and ensuring compliance with federal and institutional regulations.
Salary not listed
The Clinical Research Assistant supports clinical research by identifying eligible participants, conducting protocol-specific testing, and documenting visits. They are responsible for maintaining study documents, ensuring data accuracy, and adhering to federal and institutional regulations.
Cedars-Sinai
Perform blood collection procedures including venipuncture and skin punctures while ensuring specimen integrity. Responsibilities include accurately labeling, distributing laboratory specimens, and maintaining sanitary collection areas.
$24 - $37 / HOUR
3 days ago
Caris Life Sciences
The Laboratory Aide provides clerical and ancillary support by receiving incoming clinical specimens and transporting cases between laboratory departments. They are also responsible for the proper audit and disposal of biohazardous materials and documenting activities in the LIS.
University of Florida
Coordinates clinical research protocols by recruiting participants, managing informed consent, and ensuring regulatory compliance. Acts as a liaison between investigators, sponsors, and IRBs while managing study documentation and finances.
$53,000 - $57,000 / YEAR
US Digestive Health
The Clinical Research Coordinator assists the Research Department with patient recruitment, data management, and the collection and processing of biological specimens. They are responsible for maintaining regulatory documents, ensuring data integrity, and coordinating study visits according to strict protocols.
Alcanza Clinical Research
The coordinator is responsible for designing, updating, and controlling electronic and paper source documents for clinical trials in compliance with GCP and 21 CFR Part 11. They collaborate with site teams to ensure all protocol-defined data is accurately captured and maintained throughout the study lifecycle.
Rovia Clinical Research
The Clinical Research LPN coordinates and executes ophthalmology clinical trials following study protocols and regulatory guidelines. Key duties include conducting patient visits, performing clinical tasks, and ensuring accurate data entry and documentation.
ALLIANCE CLINICAL LLC
The Assistant Clinical Research Coordinator supports the planning and execution of clinical trials by recruiting participants and collecting research data. They ensure all study activities comply with protocols, regulatory requirements, and institutional policies to maintain data integrity and participant safety.
$20 - $26 / HOUR
Headlands Research
The CRC manages Phase I-IV clinical studies from site initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Manage and execute Phase I-IV clinical studies from site initiation to close-out in compliance with FDA and GCP guidelines. Coordinate subject visits, maintain accurate documentation, and collaborate with investigators and sponsors.
Iterative Health
The specialist assists research sites with the conduct and compliance of Phase 2-4 pharma sponsored research studies. Key duties include managing essential regulatory documents, facilitating IRB submissions, and participating in monitor visits and audits.
Care Access
The Clinical Research Assistant supports the research process by recruiting participants, conducting screenings, and obtaining informed consent. They are responsible for performing visit procedures, collecting specimens, and maintaining accurate study documentation in compliance with FDA and ICH guidelines.
$19 - $33 / HOUR
ICON plc
Serve as the primary contact between investigational sites and sponsors while conducting various site visits including selection, initiation, and close-out. Ensure site compliance with ICH-GCP and regulations while managing data quality and patient safety reporting.
$91,336 - $114,170 / YEAR
4 days ago
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.
$110,520 - $138,150 / YEAR
Mass General Brigham
Coordinates individual stroke clinical trials and supports the administrative needs of the New England Regional Coordination Center. Responsibilities include recruiting patients, collecting data, performing clinical tests, and ensuring regulatory compliance.
$24 - $39 / HOUR
