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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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The Ohio State UniversityNew
Provide support for clinical research studies within the Division of Cardiovascular Medicine, including study implementation and coordination. Responsibilities include recruiting participants, performing diagnostic testing, and managing clinical research data.
5000 Wellstar Medical Group, LLCNew
The Psychometrist I administers and scores psychological tests while assisting psychologists in conducting clinical evaluations. They are responsible for gathering patient information, maintaining accurate medical records, and synthesizing data into comprehensive reports.
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
UVA HealthNew
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
$28 - $81,500 / HOUR
The coordinator will recruit, screen, consent, and enroll participants across multiple cancer clinical trials while building relationships with study participants. Key duties include coordinating study visits, collecting high-quality data, maintaining accurate documentation, processing specimens, tracking adverse events, and ensuring protocol compliance.
$28 - $82 / HOUR
Baylor Scott & White HealthNew
The GI Psychologist will provide comprehensive behavioral health care and consultation within an outpatient specialty center, focusing on the brain-gut connection. They will collaborate with a multidisciplinary team to manage patients with chronic functional GI conditions and contribute to clinical research initiatives.
Syneos HealthNew
The Medical Assistant will ensure the safety and well-being of study participants while performing clinical tasks and supporting clinical trials. They will also guide participants through the informed consent process and manage study supplies.
$35,600 - $60,400 / YEAR
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
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
ICON plc
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$91,336 - $114,170 / YEAR
Mass General Brigham
The Clinical Research Coordinator supports oncology clinical trials by enrolling eligible patients and scheduling all protocol-mandated tests. Responsibilities include coordinating patient appointments, processing tissue and blood samples, and maintaining communication with enrolled participants.
$29 / HOUR
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
Professional Case Management
Responsible for scheduling and conducting mobile clinical visits for adolescent study participants. Tasks include performing physical assessments, phlebotomy, and submitting accurate source documentation.
$55 / HOUR
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 Clinical Research Coordinator will assist with clinical research studies, including recruiting and consenting patients, collecting data, and performing clinical tests. They will also manage IRB protocols and support various research projects related to military service-related conditions.
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.
The coordinator assists with clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. They are also responsible for performing clinical tests like phlebotomy and EKGs and maintaining regulatory documentation.
University of Virginia
Coordinate all aspects of complex clinical research projects from start-up through archiving, including patient recruitment and regulatory compliance. Manage multiple trials simultaneously while collaborating with physicians and sponsors to ensure audit-ready documentation.
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.
