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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
St. Elizabeth Healthcare
Coordinate clinical research studies by managing subject enrollment, data collection, and regulatory compliance. Collaborate with physicians to open new studies and ensure adherence to protocol and FDA guidelines.
16 days ago
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
St. Joseph Hospital & Medical Center
The role involves executing clinical research studies by screening participants, monitoring well-being, and collecting study data. The RN ensures strict compliance with federal and state regulations, including FDA and IRB guidelines.
$32 - $48 / HOUR
24 days ago
Baptist Health South Florida
The Nurse Research Coordinator supports the Clinical Research staff by coordinating and administering clinical study protocols in cooperation with the Principal Investigator. This role includes ensuring compliance with regulatory requirements and maximizing subject participation in cardiovascular research protocols.
26 days ago
University of New Mexico
Coordinate and manage regulatory compliance and documentation for pediatric oncology/hematology clinical research studies. Facilitate trial start-up and maintenance while providing technical assistance to research staff on IRB and regulatory requirements.
$3,845 - $5,399 / MONTH
1 month ago
Medical University of South Carolina
The coordinator manages pre-award grant processes, including budget development and proposal submission. They also ensure regulatory compliance by managing IRB documentation and adhering to FDA and GCP requirements.
$37,200 - $59,500 / YEAR
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
ETSU
The coordinator will facilitate specimen accrual for translational studies by recruiting subjects and obtaining informed consent. They are responsible for collecting and processing clinical samples for use or transport.
$47,002 / YEAR
Ann & Robert H. Lurie Children's Hospital of Chicago
The Research Coordinator II will manage research projects, including participant recruitment, data collection, and quality assurance. They will also coordinate with clinical partners and community organizations to ensure adherence to study protocols.
$49,920 - $81,619 / YEAR
The Clinical Research Coordinator manages the administration of multiple research studies, ensuring protocol adherence and regulatory compliance. Key duties include recruiting and screening participants, collecting study data, and maintaining communication with sponsors and investigators.
Coordinates behavioral research projects by managing study start-up, regulatory documentation, and participant recruitment. Conducts research visits, administers behavioral interventions, and performs data entry and quality assurance under PI supervision.
Hoag
The Clinical Research Coordinator RN manages all aspects of FDA-regulated clinical trials, from protocol review and subject recruitment to data collection and regulatory maintenance. They work closely with study physicians to ensure the accurate execution of Phase I-IV trials and maintain compliance with Good Clinical Practices.
$49 - $76 / HOUR
Chandler Regional Medical Center
The Clinician Research Nurse supports and executes clinical research studies by managing participant care, screening, and education. They are responsible for ensuring data integrity, monitoring for adverse events, and maintaining compliance with federal and state research regulations.
Lurie Children's Hospital
The Behavioral Research Coordinator II manages research projects, including study start-up, protocol coordination, and regulatory documentation. They also conduct research visits, facilitate behavioral interventions, and perform data abstraction and quality assurance checks.
The Behavioral Research Coordinator II manages research projects, including study start-up, protocol coordination, and regulatory compliance. They also conduct research visits, facilitate behavioral interventions, and perform data analysis under the supervision of the Principal Investigator.
HonorHealth
The coordinator facilitates regulatory affairs for clinical research, ensuring compliance with FDA, ICH, and IRB standards. They manage study protocols from startup through closure, including document preparation and regulatory correspondence.
The Behavioral Research Coordinator II manages multi-site HIV prevention and treatment trials, overseeing study operations from start-up to close-out. They are responsible for participant recruitment, regulatory documentation, data collection, and the delivery of behavioral interventions.
The Clinical Research Coordinator III is responsible for managing all aspects of complex clinical research trials, including drug, device, and biologic studies, while collaborating with physicians and stakeholders. Key duties involve conducting protocol review, administering informed consent, recruiting subjects, ensuring accurate data collection, completing CRFs, and overseeing adverse event reporting and subject follow-up.
$39 - $59 / HOUR
2 months ago
PIH Health
The Clinical Research Nurse coordinates patient care and clinical trial support within a hospital-based research setting. They ensure studies comply with federal regulations, GCP, and ethical standards while maintaining data integrity and patient safety.
$53 - $84 / HOUR
