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UTHealth Houston
Overview
The Research Coordinator III manages clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. They serve as a primary liaison between investigators, sponsors, and regulatory bodies to ensure study milestones are met.
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Compensation
Salary not listed
Posted
11 days ago
BMC Software
The Clinical Research Coordinator II manages research activities including patient recruitment, informed consent, and the processing of biological specimens. They are responsible for maintaining patient databases, entering data into electronic capture forms, and assisting with regulatory submissions and audits.
$42,500 - $59,500 / YEAR
18 days ago
University of Miami
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.
25 days ago
Tulane University
Coordinate day-to-day operations for cardiovascular disease studies, acting as a liaison between patients, investigators, and sponsors. Responsibilities include screening and enrolling patients, ensuring protocol compliance, and managing regulatory documentation.
28 days ago
Kettering Health
The Clinical Research Coordinator I assists investigators in executing research trials by screening and enrolling subjects and ensuring protocol compliance. They are responsible for data reporting, adverse event tracking, and maintaining regulatory files in accordance with GCP guidelines.
IRONWOOD PHYSICIANS,P.C.
Manages and coordinates all clinical and administrative aspects of conducting clinical trials in accordance with protocol guidelines and federal regulations. Acts as a liaison between investigators, sponsors, and the IRB while performing patient procedures and assessments.
29 days ago
UTHealth (University of Texas Health Science Center at Houston)
Coordinate and manage clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. Serve as a liaison between investigators and sponsors while managing study documentation and reporting.
1 month ago
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
US Foot & Ankle Specialists
The Clinical Research Coordinator manages and conducts clinical research projects by leading trial operations, collecting data, and ensuring strict adherence to Foot and Ankle Specialists of the Mid-Atlantic (FASMA) Standard Operating Procedures (SOPs). Key duties include monitoring study activities for compliance, maintaining detailed study records, managing subject enrollment, and acting as a liaison between investigators, the IRB, CRO, and sponsor.
2 months ago
Medical University of South Carolina
The Program Coordinator RN will provide comprehensive clinical, regulatory, and program coordination support for human subject research under the direction of the Principal Investigator and Program Manager. Responsibilities include site management, participant recruitment, scheduling visits, data collection, lab processing, conducting research protocols, and maintaining regulatory files.
3 months ago
The Clinical Research Coordinator manages and conducts clinical research projects, leading trial operations, collecting data, and ensuring strict adherence to Foot and Ankle Specialists of the Mid-Atlantic (FASMA) Standard Operating Procedures (SOPs). Key duties include acting as a liaison between investigators, sponsors, and regulatory bodies, maintaining all required study documentation, and overseeing subject enrollment and data entry.
4 months ago
The Clinical Research Coordinator manages and conducts clinical research projects by leading trial operations, ensuring adherence to Standard Operating Procedures (SOPs), and acting as a liaison between investigators, sponsors, and regulatory bodies. Key duties include monitoring study activities, maintaining detailed records, managing subject enrollment, and handling adverse event reporting.
