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University of Virginia
Overview
Coordinate all aspects of complex clinical research projects from start-up through archiving, including patient recruitment and regulatory compliance. Manage multiple trials simultaneously while collaborating with physicians and sponsors to ensure audit-ready documentation.
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Compensation
Salary not listed
Posted
3 days ago
Mass General Brigham
This role supports research studies in Sleep and Circadian Disorders by instructing subjects, obtaining informed consent, collecting, organizing, and analyzing study data, and preparing regulatory documentation. Responsibilities also include creating REDCap surveys and databases, training personnel, and troubleshooting specialized data collection devices during various shifts.
$20 - $29 / HOUR
UVA Health
The coordinator will manage multiple complex clinical trials from start-up through archiving, including patient recruitment and regulatory documentation. They will collaborate with physicians and sponsors to ensure trials are conducted according to FDA and NIH requirements.
4 days ago
University of Rochester
This role coordinates human subject research activities within the Department of Urology, focusing on screening, consenting subjects, maintaining documentation, and managing data collection according to research protocols. The specialist ensures research activities adhere to institutional policies, IRB requirements, and study protocols while coordinating with the Principal Investigator and other study team members.
$21 - $30 / HOUR
9 days ago
Visionary Ophthalmology
The coordinator manages day-to-day activities for ophthalmology clinical trials, including subject visits and regulatory compliance. They are responsible for data entry, maintaining study binders, and communicating with sponsors and CROs.
$25 - $30 / HOUR
UTHealth Houston
Identify and recruit participants for cancer screening and HPV vaccination programs within the greater Houston area. Deliver educational sessions and provide follow-up health coaching and navigation to help participants overcome barriers to care.
11 days ago
Nevada System of Higher Education
The Research Coordinator will support the Stress, Pregnancy, & Health (SPAH) Kids study by managing IRB documentation, recruiting participants, and administering cognitive and psychosocial assessments. Additionally, the role involves data management, assisting with manuscript preparation, and coordinating grant-related activities.
$25 - $37 / HOUR
Coordinate data collection and operations for the SNAK clinical trial, focusing on participant recruitment, enrollment, and retention. Manage study data, administer surveys, and connect families to community-based resources under the supervision of the Primary Investigator.
12 days ago
Duke Careers
The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.
$21 - $31 / HOUR
13 days ago
The Clinical Research Coordinator will manage study operations, including recruitment, participant engagement, and regulatory compliance for the Cancer Control and Population Sciences program. They will also ensure data integrity, maintain regulatory documentation, and serve as a liaison between investigators, sponsors, and study participants.
$59,829 - $99,960 / YEAR
The Lab Specialist will provide technical lab support by performing high-quality lab and research tasks, including processing bio-specimens, managing clinical databases, and assisting with research evaluation. Key duties involve recruiting, screening, and enrolling study participants, collecting data via interviews, obtaining informed consent, and coordinating sample collection from clinics.
14 days ago
Cedars-Sinai
Lead quantitative and qualitative research projects focused on behavioral health interventions for LGBTQ+ communities of color. Establish study SOPs, manage participant engagement, and collaborate with interdisciplinary teams and community stakeholders.
$30 - $45 / HOUR
17 days ago
UCSF
The coordinator manages clinical and translational projects, acting as a link between clinicians, research teams, and regulatory authorities. Key duties include overseeing data and specimen management, maintaining regulatory documents, and ensuring IRB compliance.
University of Miami
The therapist provides therapeutic care for children and families, specializing in Parent-Child Interaction Therapy (PCIT) to treat behavioral and emotional disorders. Responsibilities include conducting assessments, developing treatment plans, and collaborating with multidisciplinary teams to ensure coordinated psychosocial services.
18 days ago
Hospital for Special Surgery
Coordinates clinical research activities for the ARJR service, serving as a liaison between investigators, sponsors, and CROs. Manages all phases of study conduct, including recruitment, enrollment, regulatory compliance, and data maintenance.
Albert Einstein College of Medicine
The Study Coordinator manages asthma-related research projects by overseeing participant recruitment and ensuring data integrity. They serve as a liaison between stakeholders and handle regulatory documentation for the IRB and funding agencies.
$58,500 / YEAR
22 days ago
University of New Mexico
The role involves facilitating Group Assisted Psilocybin Assisted Therapy for PTSD, including preparatory, medication, and integration sessions. Responsibilities also include documenting study visits in REDCap and evaluating participants for clinical risks.
$34 - $48 / HOUR
23 days ago
University of Washington
The Research Coordinator supports translational and clinical research studies by screening patients for eligibility and obtaining informed consent. They are also responsible for processing human biospecimens and managing study data within electronic capture systems.
$55,944 - $90,000 / YEAR
New York State Psychiatry Institute
The Research Coordinator will assist with study implementation, regulatory management, and participant coordination. They will oversee daily trial operations and ensure protocol adherence.
$46,021 - $54,975 / YEAR
25 days ago
The Clinical Research Support Specialist assists in the recruitment, screening, and enrollment of study participants while managing data collection and regulatory documentation. They also conduct community outreach, schedule research visits, and maintain consistent communication with participants to ensure study adherence.
