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Beacon Clinic
Overview
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.
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Compensation
Salary not listed
Posted
2 days ago
Bausch+Lomb Companies Inc.
The Senior Principal Research Optometrist will design and lead clinical studies to support the development and launch of innovative eye care products. This role involves applying clinical and research expertise to study design, data analysis, and collaboration across functions.
$130,000 - $200,000 / YEAR
9 days ago
University of Texas Medical Branch (UTMB)
The coordinator obtains human subject data according to study protocols and manages general administrative duties to support clinical research. Key tasks include recruiting participants, maintaining regulatory documentation, and processing laboratory specimens.
16 days ago
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
21 days ago
University of Massachusetts Medical School
The Research Nurse Coordinator is responsible for conducting complex protocols related to investigational drugs and devices, acting as a liaison between various stakeholders to ensure compliance with good clinical practice standards. They perform tasks such as patient screening, documentation of study events, and regulatory paperwork management throughout the study lifecycle.
The Research Nurse Coordinator is responsible for carrying out delegated tasks related to complex protocols testing investigational drugs and devices. They act as a liaison between various stakeholders to ensure good clinical practice standards throughout the study lifecycle.
$34 - $53 / HOUR
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
22 days ago
Providence
Coordinates and maintains diverse activities for neurology clinical research trials, ensuring protocol adherence and timely study completion. Acts as a liaison for regulatory documents and manages subject recruitment, informed consent, and study documentation.
$32 - $49 / HOUR
UCSF
Execute and coordinate research protocols for the GI Oncology program, managing data collection and specimen management. The role involves ensuring regulatory compliance, maintaining databases, and acting as an intermediary between various departments.
$32 - $45 / HOUR
23 days ago
DM CLINICAL RESEARCH GROUP
The Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products as part of clinical research trials and ensuring compliance with study-specific blinding plans. They will also supervise medication records, assist in training new team members, and interact with various stakeholders to ensure protocol adherence.
24 days ago
Ochsner Health
This role manages and executes clinical trial activities, including patient recruitment, screening, and the administration of investigational therapies. The researcher serves as a liaison between patients and principal investigators while ensuring strict adherence to Good Clinical Practice guidelines.
25 days ago
University of Miami
The specialist is responsible for collecting, analyzing, and documenting research data while supporting daily study activities and statistical needs. Key duties include patient recruitment for glaucoma studies, maintaining study logs, and coordinating with community partners and clinic staff.
Baptist Health South Florida
The Research Nurse is responsible for enlisting patients into clinical trials and ensuring strict adherence to study protocols and regulatory standards. They collaborate with physicians to determine patient eligibility and provide essential education to both staff and patients.
$73,861 - $98,235 / YEAR
26 days ago
The coordinator will act as the primary recruiter, screening and enrolling participants for a phase 1 HIV prevention clinical trial. Responsibilities include managing study visits, data integrity, IRB requests, and coordinating staff and interns.
$38 / HOUR
29 days ago
Beth Israel Lahey Health
The Clinical Research Coordinator II is responsible for coordinating and administering multiple research studies, ensuring adherence to protocols and regulatory requirements. This role involves working closely with principal investigators and research staff, as well as interacting with study participants diagnosed with cardiovascular disease.
$19 - $31 / HOUR
1 month ago
Johns Hopkins University
The coordinator administratively manages clinical protocol implementation, ensuring adherence to study guidelines and validity of findings. Responsibilities include participant recruitment, consenting, data collection, and the processing and tracking of biospecimens.
$17 - $30 / HOUR
Cincinnati Eye Institute
The Clinical Research Coordinator oversees study protocols, ensures regulatory compliance, and manages site activities including patient recruitment and data documentation. They also coordinate with sponsors, manage study budgets, and perform study-specific testing and exams according to protocol guidelines.
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The Clinical Research Coordinator manages and executes clinical research protocols for breast oncology trials, overseeing administrative tasks, data integrity, and patient scheduling. They act as a liaison between sponsors and research staff while ensuring compliance with regulatory policies and assisting in patient care.
$40 - $45 / HOUR
