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The Ohio State UniversityNew
Overview
Provide support for clinical research studies within the Department of Internal Medicine, specifically in Gastroenterology, Hepatology, and Nutrition. Responsibilities include coordinating study implementation, recruiting participants, performing diagnostic testing, and managing research data.
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Compensation
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Posted
New
Orlando HealthNew
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.
Professional Case ManagementNew
The Certified Mobile Research Nurse is responsible for scheduling and conducting mobile visits for pediatric study participants. They must perform physical assessments, collect specimens, and submit accurate source documentation in coordination with project managers.
$65 / HOUR
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
Mass General Brigham
Coordinate NIH-funded studies on substance use disorder by managing participants, data, and IRB correspondence. Perform clinical tests such as phlebotomy and EKGs while maintaining study documentation and regulatory binders.
$29 / HOUR
Beacon Clinic
Coordinates daily clinical trial activities, ensuring compliance with FDA and OHRP regulations while managing participant screening and data submission. Performs medical assistant duties including phlebotomy, vital signs documentation, and assisting providers with exams.
The coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They are also responsible for maintaining study documentation, ensuring regulatory compliance, and assisting with grant or journal submissions.
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
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.
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
