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Arizona Liver HealthNew
Overview
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.
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Compensation
$28 - $36 / HOUR
Posted
New
Headlands Research
The Clinical Research Coordinator manages all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. They are responsible for subject visits, accurate documentation, data entry, and maintaining effective communication with investigators and sponsors.
Salary not listed
9 days ago
ObjectiveHealth
Coordinate and manage clinical trials by handling patient identification, screening, enrollment, and conducting clinic visits. Perform direct patient care activities including blood draws, ECGs, and medication administration while ensuring strict protocol adherence.
21 days ago
Alcanza Clinical Research
The Clinical Research Nurse ensures the execution of assigned studies by performing clinical procedures and patient follow-ups. Responsibilities include screening patients, documenting in source charts, and maintaining compliance with FDA and GCP regulations.
23 days ago
The coordinator is responsible for managing assigned clinical studies, including patient identification, screening, enrollment, and conducting clinic visits. They must ensure strict protocol adherence, maintain clean data entry, and foster relationships between PIs, sponsors, and monitors.
28 days ago
The coordinator is responsible for managing assigned clinical studies, including patient identification, screening, and enrollment. They perform direct patient care activities and ensure strict adherence to IRB protocols and regulatory requirements.
The coordinator is responsible for managing assigned clinical studies, including patient identification, screening, enrollment, and conducting clinic visits. They must ensure strict protocol adherence and maintain clean data entry while fostering relationships between PIs, sponsors, and monitors.
Coordinate clinical trial protocols including patient identification, screening, enrollment, and conducting clinic visits. Perform direct patient care activities and maintain strict regulatory compliance and data accuracy for assigned studies.
Fortrea
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management for oncology clinical trials. Ensures data integrity, patient protection, and adherence to protocol and regulatory requirements.
$115,000 - $140,000 / YEAR
1 month ago
Responsible for all aspects of clinical site monitoring, including routine visits, close-outs, and site management. Ensures patient protection, data integrity, and adherence to study protocols and regulatory requirements.
Alliance For MultiSpecialty Research LLC
Manages clinical research study tasks with a specialized focus on investigational product handling, administration, and subject safety. Coordinates trial activities in compliance with FDA regulations, GCP guidelines, and protocol-specific requirements.
University of Kansas Medical Center
Coordinate all aspects of clinical trial activities within the Neuromuscular Disease Program, including patient recruitment and study visit management. Ensure strict adherence to sponsor protocols and regulatory requirements while managing data entry and IRB submissions.
$60,800 - $91,200 / YEAR
The role involves leading and supporting clinical trial monitoring activities, ensuring high standards of care for participants, and responding to emergencies based on clinical research standards. Responsibilities cover all aspects of study site monitoring, including routine monitoring, close-out visits, vendor liaison, and comprehensive site management as per project plans.
$105,000 - $117,000 / YEAR
ALLIANCE CLINICAL LLC
The Clinical Research Coordinator manages clinical trial visits, data collection, and participant health monitoring while ensuring adherence to protocols. They collaborate with the Principal Investigator to maintain study integrity and comply with Good Clinical Practice guidelines.
$27 - $33 / HOUR
The CRA is responsible for all aspects of study site monitoring, including routine visits, site management, and ensuring protocol adherence. They also manage data integrity, handle serious adverse event reporting, and coordinate clinical projects as a local contact.
$105,000 - $145,000 / YEAR
2 months ago
University of Colorado
The primary responsibility is serving as a Clinical Research Coordinator, overseeing day-to-day operations for multiple clinical trials and ensuring alignment with established protocols. Key duties include subject recruitment, executing informed consent, performing study procedures like phlebotomy, and managing data entry into CRFs.
$48,446 - $60,000 / YEAR
3 months ago
