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American Addiction Centers
Overview
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
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Compensation
$31 - $46 / HOUR
Posted
2 days ago
M3USA
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
Salary not listed
1 month ago
Pharmaron
The Clinical Regulatory Associate manages essential clinical trial documentation, IRB submissions, and study start-up activities. They ensure compliance with GCP, GLP, and internal procedures while supporting monitoring visits and study closeout activities.
$50,000 - $54,000 / YEAR
Peregrine Team
The Clinical Research Coordinator will manage daily clinical trial activities, including patient scheduling and regulatory compliance. They will also serve as a key liaison between investigators, sponsors, and patients while ensuring accurate data entry into EDC systems.
Medpace, Inc.
The Study Start-Up Coordinator communicates with research sites to collect essential documents for clinical trials and maintains quality reviews of trial documents. They also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also provide guidance to ensure compliance with regulations and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality review of trial documents. They will also manage timelines for study start-up through collaboration with internal teams.
Joslin Diabetes Center
The Clinical Research Coordinator manages clinical research projects by coordinating study visits, obtaining informed consent, and ensuring adherence to protocols and regulatory guidelines. They are responsible for collecting primary data, processing laboratory samples, and maintaining accurate regulatory documentation for study sponsors and IRBs.
$22 - $24 / HOUR
2 months ago
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.
Alliance for Clinical Trial in Oncology Foundation
The Clinical Research Associate will manage clinical trial operations, including site selection, study start-up, and maintenance of trial master files. They will collaborate with CROs and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards.
IQVIA
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
$71,900 - $145,300 / YEAR
UVA Health
Coordinates and implements clinical trial research studies within the Department of Plastic Surgery, working closely with Principal Investigators. Responsibilities include managing IRB protocols, patient recruitment, data collection, and regulatory documentation.
Ann & Robert H. Lurie Children's Hospital of Chicago
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
Lurie Children's Hospital
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
Alcanza Clinical Research
The Clinical Research Coordinator ensures the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs, involving tasks like patient screening, consent, follow-up visits, and meticulous documentation in source charts and EDC systems. Responsibilities also include performing basic clinical procedures such as vital signs, ECGs, and potentially blood specimen collection, storage, and shipping.
CenExel
The Study Start-Up Assistant performs routine administrative and clerical tasks such as file organization, preparing reports or correspondence, and providing administrative support to ensure efficient office operations. Essential duties include managing communications, handling information requests, performing general clerical duties, and resolving administrative inquiries.
