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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
Vanderbilt University Medical Center
Coordinate clinical trial protocols, patient consent processes, and the preparation of IRB and regulatory documents. Identify and recruit research subjects while managing data collection and lab specimen shipping.
Salary not listed
7 days ago
Shriners Children's
The Administrative Assistant supports research operations by coordinating office services, purchasing, payroll, and credentialing for scientific staff. They also manage research grant activities, including application planning, submission adjustments, and statistical summaries.
$26 - $38 / HOUR
24 days ago
University of Florida
The coordinator will manage participant recruitment, administer cognitive and clinical assessments, and handle MRI/PET scans. Additional duties include managing IRB documentation, data entry, and preparing progress reports for the NIH.
$37,000 - $47,000 / YEAR
28 days ago
Mount Sinai Health System
The Research Program Coordinator develops and participates in study protocols, designs management and statistical plans, and analyzes data. They are responsible for conducting human subjects or laboratory research and preparing final study reports.
$58,661 - $81,675 / YEAR
1 month ago
UCSF
The Clinical Research Coordinator supports the management of various clinical trials by ensuring protocol initiation and regulatory compliance. They are responsible for maintaining study records, collecting data, and reporting progress to the Principal Investigator.
$38 - $61 / HOUR
The Research Program Coordinator develops and participates in study protocols, designs management and statistical plans, and analyzes data. They are also responsible for preparing final reports and overseeing human subjects or laboratory research activities.
The Clinical Research Coordinator will assist in daily research activities, including obtaining informed consent, collecting study data, and maintaining records. They will also support participant recruitment, scheduling, and the preparation of grant and regulatory documents.
Nationwide Children's Hospital
This role involves performing complex administrative activities for a Section Chief or VP, including scheduling appointments, managing comprehensive travel arrangements, and processing reimbursements. The position also requires coordinating special projects and creating moderately complex documents like correspondence, spreadsheets, and visual presentations.
UT Southwestern Medical Center
The Regulatory Associate Senior manages regulatory support for clinical trials, including protocol review, IRB/IACUC submissions, and maintenance of essential regulatory documents. They also provide technical consultation to investigators, train staff on compliance, and mentor junior team members.
2 months ago
The Regulatory Associate Senior manages regulatory submissions for clinical trials, including protocol reviews, consent form drafting, and IRB/FDA filings. They also provide technical consultation to investigators and mentor junior staff on regulatory compliance and research policies.
Emory University
The Clinical Research Coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and maintaining study documentation. They also perform clinical tasks such as specimen collection, phlebotomy, and monitoring regulatory submissions.
University of Colorado
The Regulatory Affairs Coordinator independently manages all IRB and regulatory processes for ophthalmology research studies. Responsibilities include preparing regulatory submissions, maintaining investigator site files, and ensuring compliance with institutional and federal regulations.
$59,995 - $87,761 / YEAR
PAVIR
The Clinical Research Assistant will coordinate clinical studies on dementia and aging, including patient recruitment, data management, and regulatory compliance. They will also conduct community outreach and educational events to increase dementia awareness among Veterans and their families.
Johns Hopkins University
The role involves triaging and delivering substance use/mental health screenings and clinical assessments to youth and families, followed by providing case management, counseling, and coordination of services. Responsibilities also include implementing brief interventions for substance use using motivational interviewing techniques and developing tailored prevention and treatment plans.
$20 - $35 / HOUR
The Senior Research Assistant will independently conduct operational and technical activities for the ENSPIRE project, which focuses on economic empowerment and sexual/reproductive health among young adults. Specific duties include developing data collection tools, overseeing data collection and analysis, conducting participant recruitment and interviews, and co-leading educational sessions.
$41,300 - $72,300 / YEAR
This role involves the administrative coordination of research protocol implementation, ensuring efficient logistical execution of study activities and providing administrative support for all related matters. Key duties include coordinating study activities to maintain finding validity, developing operational plans with senior staff, and overseeing data collection and record management.
$17 - $30 / HOUR
TriHealth
The coordinator manages all components for successful clinical research trials, functioning as an educator, consultant, and liaison while ensuring safety, integrity, and efficiency by applying knowledge of good clinical practices. This involves coordinating Phase II through IV trials from initial sponsor contact through study completion and close-out, including marketing and determining protocol feasibility.
NCIRE - The Northern California Institute for Research and Education, Inc.
The Staff Research Associate will assist the Principal Investigator and Study Coordinators with the execution of daily operations for NIH and DoD funded epidemiological research projects focused on dementia risk and prevention. Key duties include subject recruitment, data management, literature reviews, manuscript development, and general research administrative tasks.
$25 - $41 / HOUR
3 months ago
The Physical Therapist is responsible for the evaluation, treatment planning, and implementation of treatment for all referred patients, ensuring they reach their optimal physical functioning level. This role also involves maintaining accurate documentation, communicating treatment plans to patients and families, and ensuring departmental efficiency and safety.
