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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
The coordinator supports the GROWTH study by managing regulatory documents, recruiting eligible subjects, and collecting and processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
24 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.
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 coordinator supports clinical trials for rare genetic disorders by managing regulatory documents, recruiting subjects, and processing specimens. They collaborate with sponsors and CROs to ensure study timelines are met and data is accurately entered into electronic platforms.
$22 - $36 / HOUR
This 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.
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.
Coordinates clinical research activities, including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
Coordinates clinical research activities including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
Assists investigators in the implementation and coordination of clinical research activities, including regulatory document maintenance and subject recruitment. Responsible for collecting specimens, abstracting medical data, and facilitating study monitoring visits.
The Clinical Research Coordinator assists investigators with the implementation and conduct of clinical research activities, including regulatory document maintenance and patient recruitment. They are also responsible for specimen collection, data entry into electronic capture systems, and monitoring study visits.
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.
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 Clinical Research Coordinator assists investigators with study start-up, regulatory documentation, and the implementation of clinical research protocols. They are responsible for patient recruitment, specimen processing, data entry, and facilitating study visits while ensuring adherence to research ethics.
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.
Danbury Hospital
The Clinical Research Coordinator collaborates with leadership to manage all aspects of clinical research studies, including patient recruitment and protocol implementation. Responsibilities also include data collection, query resolution, and ensuring compliance with regulatory agencies and the Institutional Review Board.
$30 - $56 / HOUR
2 months ago
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.
