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Orlando HealthNew
Overview
Develop and implement administrative strategies to manage clinical trials and coordinate large-scale research studies. Responsibilities include assessing patient eligibility, monitoring adverse reactions, and ensuring adherence to FDA and protocol guidelines.
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Compensation
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UTHealth HoustonNew
Assists with the conduct and management of human subject research projects, including participant recruitment and data collection. Responsible for maintaining databases, preparing progress reports, and supporting grant proposals and regulatory submissions.
Mass General BrighamNew
Coordinate and run study visits involving neuroimaging and biological sample collection for infection-associated health conditions. Manage IRB compliance documents, screen potential participants, and assist with data processing and analysis.
$21 - $29 / HOUR
Arizona Liver HealthNew
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
$28 - $36 / HOUR
University of Massachusetts Medical SchoolNew
The Research Associate I provides operational support to the laboratory by performing experiments and maintaining accurate research records. They are responsible for interpreting data, monitoring supply levels, and ensuring compliance with safety and institutional protocols.
Duke Careers
Perform technical and clerical duties to support clinical research, including participant recruitment, data collection, and specimen processing. Ensure compliance with regulatory policies and assist in the preparation of IRB documentation and study reports.
$20 - $31 / HOUR
2 days ago
Mass General Brigham
The Clinical Research Coordinator manages day-to-day operations of clinical research studies, including participant recruitment, data collection, and study visit coordination. They ensure protocol compliance and handle regulatory documentation and IRB submissions.
$29 / HOUR
ICON plc
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
$110,520 - $138,150 / YEAR
Manages cardiovascular clinical trials, including subject recruitment, enrollment, and the maintenance of regulatory documentation. Performs clinical tests such as phlebotomy and EKGs while managing research data and biological samples.
$20 - $29 / HOUR
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.
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
Children’s Hospital of Philadelphia
Perform complex research procedures and experiments focusing on epigenetic mechanisms of brain injury. Manage animal colonies, maintain laboratory inventory, and assist in writing grants and journal articles.
$43,900 - $53,440 / YEAR
IQVIA
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
$33,000 - $82,600 / YEAR
The coordinator manages clinical research studies on depression, focusing on participant recruitment, screening, and the administration of assessments. They are also responsible for data collection, maintaining regulatory binders, and contributing to scholarly manuscripts.
Iterative Health
The Research Assistant supports clinical trial activities by assisting the study team with recruitment, screening, and protocol management. They are also responsible for maintaining study documentation, managing supplies, and ensuring compliance with regulatory and site policies.
3 days ago
The Associate in Research will assist with IRB protocols, recruit and consent study participants, and perform EEG recordings and neuromodulation. They are also responsible for data compilation, report preparation, and maintaining lab records.
Children's Health
The Pathologists' Assistant is responsible for preparing, gross describing, and dissecting surgical specimens for histologic processing, including performing frozen sections and assisting in fine needle aspirations. This role also participates in the preparation and performance of postmortem examinations, including associated specialized procedures.
The Pathologists' Assistant is responsible for the preparation, gross description, and dissection of surgical specimens for histologic processing, including performing frozen sections and assisting in fine needle aspirations. This role also participates in the preparation and performance of postmortem examinations, including associated specialized procedures.
University of Tennessee
The Research Technician 2 supports research on lymphedema and AI in cancer care under the supervision of a Principal Investigator. Responsibilities include managing regulatory paperwork, IRB applications, and preparing study protocols and manuscripts.
$19 / HOUR
University of Iowa
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.
4 days ago
