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University of Massachusetts Medical SchoolNew
Overview
The Clinical Research Coordinator manages human subject research protocols, including regulatory documentation, participant visits, and data collection. They ensure compliance with federal and institutional guidelines while supporting investigators with grant preparation and study reporting.
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Compensation
Salary not listed
Posted
New
Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
7 days ago
Baylor Scott & White Health
The Clinical Research Coordinator 2 supports Principal Investigators in conducting clinical trials from pre-study implementation to closure. Key duties include managing IRB reports, developing study budgets, and coordinating protocols across various departments.
8 days ago
University of Miami
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to guidelines. This role involves ensuring participant safety, adherence to protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
12 days ago
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to regulatory guidelines. This role involves ensuring participant safety, adhering to approved protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
CenExel
Provides direct support to Clinical Research Coordinators by maintaining patient charts and preparing visit materials. Responsible for data entry, query resolution, and assisting with clinical assessments like blood pressure and urine collection.
$20 - $21 / HOUR
14 days ago
Kailera Therapeutics, Inc.
Acts as the primary liaison and subject matter expert for non-clinical pharmacology and toxicology studies conducted at external CROs. Responsible for designing study protocols, ensuring GLP compliance, and integrating toxicology data for regulatory submissions.
$127,000 - $155,000 / YEAR
17 days ago
Richmond University Medical Center
The RN Coordinator manages patient enrollment and participation in clinical research trials while ensuring adherence to study protocols and regulatory guidelines. They perform clinical assessments and maintain accurate study documentation and records.
$60 - $64 / HOUR
1 month ago
The Research Assistant I provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant visits, conduct basic assessments, and facilitate communication between study stakeholders.
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and assisting with clinical assessments. They are also responsible for data entry, query resolution, and facilitating study monitoring visits while adhering to strict research protocols.
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
Mass General Brigham
The Clinical Research Coordinator will assist with clinical research studies by recruiting and consenting patients, collecting data, and maintaining study records. They will also serve as a liaison between patients and physicians while ensuring compliance with IRB protocols and study guidelines.
$24 - $39 / HOUR
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant visits, clerical tasks, and the facilitation of study monitoring visits.
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, preparing visit materials, and assisting with clinical assessments. They also handle data entry, inventory management, and facilitate study monitoring visits while ensuring strict adherence to protocol guidelines.
AstraZeneca
You will be responsible for the preparation, initiation, monitoring, and closure of clinical study centers while ensuring compliance with international guidelines and local regulations. You will work in collaboration with the local study team to ensure quality and quantity commitments are met in a timely manner.
$101,948 - $152,922 / YEAR
2 months ago
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, preparing visit materials, and assisting with clinical assessments. They are also responsible for data entry, inventory management, and facilitating study monitoring visits.
$20 / HOUR
INNOVO RESEARCH INC
The Clinical Research Coordinator is responsible for managing clinical research data and documents, performing clinical procedures, and assisting with daily workload planning. They also recruit participants, maintain study data, and ensure compliance with regulatory requirements.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for all Case Report Forms (CRFs).
$20 - $23 / HOUR
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
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
