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Mass General Brigham
Overview
The Clinical Research Coordinator will assist with clinical research studies, including recruiting and consenting patients, collecting data, and performing clinical tests. They will also manage IRB protocols and support various research projects related to military service-related conditions.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
Systimmune
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
$70,000 - $95,000 / YEAR
9 days ago
ProHEALTH Medical Management
The Clinical Research Coordinator is responsible for coordinating clinical trials, managing patient recruitment, and conducting patient visits. Key duties include handling IRB submissions, processing laboratory specimens, and ensuring strict adherence to study protocols and federal regulations.
$26 - $38 / HOUR
13 days ago
The Clinical Research Coordinator manages patient visits, recruitment, and the logistical aspects of clinical trials in accordance with regulatory standards. They are responsible for IRB submissions, data entry, and collaborating with physicians to ensure protocol adherence.
Cedars-Sinai
Coordinates and implements complex clinical research studies by managing data collection, participant scheduling, and IRB submissions. Serves as a primary contact for sponsors and provides training to junior staff to ensure protocol compliance.
$24 - $36 / HOUR
24 days ago
Emory University
The coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and specimen collection. They also coordinate study services, maintain regulatory submissions, and monitor charges for research projects.
Salary not listed
25 days ago
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, supervising specimen collection, and ensuring strict protocol compliance.
Prisma Health
Responsible for the implementation, management, and oversight of clinical trial research studies, including patient visit management and data flow. Coordinates both investigator-initiated and industry-sponsored trials while ensuring compliance with protocols and regulatory agencies.
Assist in the coordination and implementation of noncomplex clinical research studies through data collection and participant scheduling. Support regulatory compliance by assisting with IRB submissions and maintaining study supplies.
$24 - $33 / HOUR
28 days ago
Mid Atlantic Retina
The Research Assistant supports the Research Unit in conducting clinical trials by collecting and processing clinical data. They provide administrative support, assist with patient recruitment, and maintain regulatory documentation and temperature logs.
1 month ago
The coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and specimen collection. They are also responsible for maintaining equipment, tracking regulatory submissions, and coordinating study procedures.
Ochsner Health
This role manages the initiation and maintenance of clinical trials, including participant recruitment, screening, and regulatory documentation. The coordinator serves as a liaison between patients and Principal Investigators while ensuring compliance with ethical and safety guidelines.
The coordinator manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, processing specimens, and ensuring strict protocol compliance.
IQVIA
Perform site monitoring and management to ensure study compliance with protocols, regulations, and sponsor requirements. Manage study progress, including regulatory submissions, recruitment tracking, and data integrity verification.
$64,000 - $189,000 / YEAR
Arrowhead Pharmaceuticals
Provide clinical pharmacology and pharmacometrics leadership for assigned development programs, contributing to clinical trial design and performing hands-on PK/PD analyses. Oversee the preparation of PK analysis reports and clinical pharmacology components of global regulatory submissions.
$120,000 - $170,000 / YEAR
University of Pennsylvania
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
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.
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The Clinical Research Associate I coordinates clinical study implementation, abstracts research data, and ensures compliance with federal and institutional regulations. They are responsible for completing case report forms, managing regulatory submissions to the IRB, and assisting with patient research billing.
The Clinical Research Associate is responsible for performing site monitoring visits to ensure study protocol adherence and regulatory compliance. They also manage site recruitment plans, maintain study documentation, and oversee data integrity throughout the clinical trial process.
$87,200 - $182,000 / YEAR
