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Ann & Robert H. Lurie Children's Hospital of Chicago
Overview
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
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Compensation
$49,920 - $81,619 / YEAR
Posted
6 days ago
UCSF
Perform entry-level duties to support and coordinate clinical trials, including subject recruitment, data collection, and protocol preparation. Assist in maintaining data quality within study databases and ensuring compliance with research guidelines.
Salary not listed
22 days ago
The coordinator supports clinical trials for rare genetic disorders by managing regulatory documents and recruiting eligible study subjects. They are also responsible for collecting specimens, entering data into electronic platforms, and coordinating study visits.
$22 - $36 / HOUR
27 days ago
Lurie Children's Hospital
The coordinator manages the GROWTH study by handling regulatory documents, recruiting subjects, and collecting/processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
29 days ago
Assists investigators in implementing and coordinating clinical research activities, including regulatory document maintenance and subject recruitment. Manages data entry into electronic platforms and handles specimen collection and processing.
1 month ago
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.
The role supports clinical and behavioral health research projects by assisting with study implementation, regulatory documentation, and IRB submissions. Responsibilities also include participant recruitment, data collection via REDCap, specimen processing, and maintaining study-specific records.
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, overseeing all aspects from document preparation to study conduct across departments. Responsibilities also include managing participant engagement, collecting specimens, recording data, and assisting with financial aspects like invoicing.
2 months ago
CenExel
The Research Assistant I supports Clinical Research Coordinators by creating and maintaining patient charts, preparing for participant visits, and ensuring all necessary study materials are available and accurate. Key duties also involve timely data entry, query resolution for CRFs, conducting basic participant assessments, and assisting with monitoring visits.
$19 - $21 / HOUR
US Foot & Ankle Specialists
The Clinical Research Coordinator will independently manage and execute clinical trials, overseeing day-to-day study operations, regulatory compliance, patient coordination, and data management according to protocol and guidelines. Key duties include managing the full study lifecycle from start-up to closeout, ensuring compliance, and coordinating with investigators, sponsors, and the IRB.
This role coordinates all aspects of clinical research projects, overseeing activities from study start-up through close-out while ensuring strict adherence to protocols and regulatory requirements. Key functions include managing regulatory documentation, participant engagement, data lifecycle management, and assisting with financial and dissemination activities.
$59,280 - $96,928 / YEAR
This role coordinates all aspects of clinical research projects, overseeing activities from study start-up through close-out while ensuring strict adherence to protocols and regulatory requirements. Key functions include managing regulatory documentation, participant engagement, data lifecycle management, and leading the dissemination of research findings.
3 months ago
Carbon Health
The Principal Investigator will serve as the lead for multiple clinical trials (Phases I to IV), taking responsibility for clinical research conduct, quality assurance, and supervising sub-investigators. This role involves attending site initiation visits, sponsor monitoring visits, and evaluating study volunteer eligibility according to regulations.
$200 / HOUR
Alcanza Clinical Research
The Principal Investigator is responsible for conducting and coordinating daily clinical trial activities in compliance with all relevant guidelines, protocols, and company policies. This role involves providing overall site leadership focused on enhancing efficiencies, ensuring patient safety, and maintaining protocol and regulatory compliance.
