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K2 Staffing LLCNew
Overview
The Psychometric Rater administers and interprets quantitative and qualitative tests for clinical trials focusing on neurodegenerative and mental health disorders. They are responsible for maintaining data consistency, ensuring subject safety, and coordinating with investigators and sponsors.
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Compensation
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New
Eastern Virginia Medical SchoolNew
Manages daily operations of clinical trials, acting as the primary link between investigators, participants, and sponsors. Responsibilities include participant recruitment, data collection, regulatory compliance, and monitoring participant safety.
$72,000 / YEAR
Children's Hospital of PhiladelphiaNew
The role involves the complete coordination of clinical research activities, including patient recruitment, informed consent, and adherence to IRB protocols. Responsibilities also include managing regulatory documents, collecting laboratory specimens, and ensuring GCP compliance.
$56,890 - $71,110 / YEAR
Vertex Inc.New
The Pathology Research Scientist will conduct routine and specialized histology techniques and perform wet lab work to support drug development projects. They will collaborate with other scientists and pathologists to provide high-quality data and contribute to technical documentation.
$105,600 - $158,400 / YEAR
University Retina
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.
$21 - $24 / HOUR
3 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.
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
4 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.
