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University of Miami
Overview
The coordinator manages simple clinical research protocols, including participant pre-screening, enrollment, and data collection. They are also responsible for monitoring adverse events, ensuring regulatory compliance, and maintaining study-specific regulatory binders.
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Compensation
Salary not listed
Posted
7 days ago
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.
9 days ago
The coordinator manages the day-to-day operations of clinical research protocols from initiation to close-out, ensuring participant safety and adherence to guidelines. Key duties include recruiting participants, collecting data, processing specimens, and maintaining regulatory documentation.
11 days ago
The coordinator manages entry-level clinical research activities, including participant screening, data collection, and protocol implementation. They are responsible for maintaining regulatory binders and coordinating study visits and timelines.
25 days ago
Sanford Health
Coordinates clinical research studies by managing patient contact, data collection, and adherence to research protocols. Responsibilities include screening participants, performing lab draws, and collaborating with physician investigators to ensure compliant treatment.
$28 - $44 / HOUR
The coordinator manages simple clinical research protocols, including participant screening, data collection, and maintenance of regulatory binders. They are responsible for recruiting patients, obtaining informed consent, and ensuring adherence to international and local regulatory standards.
Coordinates the planning, implementation, and monitoring of clinical research studies from initiation to close-out. Manages participant recruitment, data collection, and regulatory documentation while ensuring adherence to safety protocols.
Arkansas Children's Hospital
The Research Assistant Clinical supports various clinical trials and research studies by managing day-to-day project activities and participant recruitment. Key duties include collecting and entering study data, maintaining precise records, and ensuring adherence to regulatory guidelines.
28 days ago
Carilion Clinic
The coordinator assists with administrative activities for industry, grant, or internally funded research studies while ensuring compliance with institutional and governing policies. Key duties include recruiting participants, obtaining informed consent, collecting data, and managing regulatory documentation for the IRB and FDA.
1 month ago
The Clinical Research Coordinator supports cardiology clinical trials by managing administrative activities, recruiting participants, and ensuring compliance with regulatory guidelines. They serve as a liaison between sponsors, IRBs, and medical staff while mentoring junior coordinators and assisting in grant writing.
University of Southern California
The Protocol Coordinator manages clinical research trials by ensuring protocol compliance, coordinating patient eligibility, and monitoring adverse events. They act as a primary liaison between patients, physicians, and pharmaceutical sponsors to facilitate safe and accurate study execution.
$50 - $63 / HOUR
City of Hope
Manage clinical trial patients by assessing eligibility, monitoring treatment responses, and ensuring strict adherence to IRB protocols. Coordinate care across various settings while educating patients and families on trial procedures and informed consent.
Epicrispr Biotechnologies
The role involves supporting the execution and oversight of clinical trials, including site management and on-site sample operations. The candidate will ensure compliance with GCP guidelines and collaborate with CROs to maintain data integrity and protocol adherence.
$115,000 - $121,000 / YEAR
CenExel
The Clinical Research Coordinator II manages patient involvement and clinical trial activities while ensuring strict adherence to ICH, GCP, and protocol guidelines. They also assist with data reporting, safety assessments, and provide support to the Clinical Trial Manager in site operations.
The incumbent performs chart reviews, manages study participant eligibility, and coordinates routine clinical research activities including data collection and protocol maintenance. They also assist in monitoring adverse events and ensure compliance with international, national, and local regulatory requirements.
Fortrea
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
The Clinical Research Coordinator manages patient involvement and study data in strict adherence to ICH and GCP guidelines. They also assist with regulatory duties, safety assessments, and provide support to the Clinical Trial Manager.
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
2 months ago
PAVIR
The Clinical Research Assistant will coordinate clinical studies on dementia and aging, including patient recruitment, data management, and regulatory compliance. They will also conduct community outreach and educational events to increase dementia awareness among Veterans and their families.
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
