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Johns Hopkins UniversityNew
Overview
The coordinator manages the administrative and logistical implementation of clinical research protocols to ensure validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
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Compensation
$17 - $30 / HOUR
Posted
New
Medical University of South Carolina
The incumbent will coordinate the recruitment, screening, and enrollment of research participants while collecting psychological and biological data. They are also responsible for maintaining regulatory documentation and providing administrative support for grant proposals and publications.
$37,200 - $59,500 / YEAR
2 days ago
5000 Wellstar Medical Group, LLC
Join the Outpatient Advanced Heart Failure team to manage severe heart failure and cardiomyopathies. Collaborate with a specialized team of APPs and physicians to provide advanced treatments.
Salary not listed
4 days ago
Johns Hopkins University
Support the Pulmonary research team by implementing clinical research protocols and performing administrative operations. Responsibilities include patient screening, data collection, maintaining records, and coordinating with clinicians and program sponsors.
$15 - $23 / HOUR
15 days ago
The Research Program Assistant manages day-to-day operations for a federally funded study on opioid use disorder treatment, including coordinating trainings and meetings. They are also responsible for data collection, regulatory IRB documentation, and preparing progress reports.
16 days ago
The coordinator will administratively manage clinical protocol implementation and ensure the logistical efficiency of study activities. Key duties include recruiting participants, managing the consenting process, and handling IRB submissions and data collection.
The coordinator will administratively manage clinical protocol implementation and ensure the efficient logistical execution of study activities. Key duties include recruiting participants, managing the consenting process, and handling IRB submissions and data collection.
Sanford Health
Provide comprehensive medical oncology and hematology care, including evaluating, diagnosing, and treating patients from adolescence to adulthood. Collaborate with multidisciplinary tumor boards and participate in clinical research and teaching opportunities.
26 days ago
The Program Assistant supports research projects focused on cancer prevention and healthcare access under Dr. Trisha Amboree. Key duties include conducting surveys, assisting with data analysis, and managing grant submissions and IRB protocols.
29 days ago
Cedars-Sinai
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
Mass General Brigham
The Co-op Assistant supports clinical research studies by developing patient recruitment strategies and managing data collection. They are also responsible for processing blood samples, maintaining regulatory binders, and performing administrative scheduling tasks.
$18 - $24 / HOUR
1 month 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
Roswell Park Comprehensive Cancer Center
The successful candidate will join the surgical pathology staff to provide diagnostic services and translational research support to faculty within a collegial environment. This role involves handling a wide variety of oncologic cases from in-house and consultation practices, while also encouraging and supporting the development of an independent research program.
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
University of Oklahoma
Coordinate multiple cancer outcomes research protocols, including participant enrollment and data management using REDCap and OnCore. Collaborate with principal investigators and the IRB to develop protocols and contribute to manuscript development.
The specialist manages regulatory maintenance for oncology clinical trials, including IRB submissions and internal quality control. They also support program operations, train research staff, and facilitate compliance with institutional and federal research guidelines.
$48,000 - $84,100 / YEAR
The Research Program Coordinator manages daily logistical and operational activities for clinical research studies, including participant recruitment, enrollment, and data integrity. They also serve as a liaison between clinical staff, investigators, and community partners while ensuring adherence to study protocols and regulatory requirements.
The IIT Research Program Coordinator will manage investigator-initiated clinical trials from concept through activation and regulatory submission. They will collaborate with investigators, clinicians, and regulatory teams to ensure compliant and impactful research execution.
$38,700 - $50,300 / YEAR
Community Health Network
The Advanced Practice Provider will provide comprehensive care for patients undergoing stem cell transplant and cellular therapy. They will collaborate with a multi-disciplinary team including medical oncologists, surgeons, and research staff to deliver state-of-the-art cancer treatment.
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.
