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Responsibilities Prepare, submit, and manage IRB applications (new studies, amendments, continuing reviews, and adverse event reports) in compliance with institutional policies and federal regulations Conduct and support study procedures, including participant screening, recruitment, scheduling, informed consent, interviews, assessments, specimen collection, and assisting with EEG/MRI and other protocol-required acti

Responsibilities Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations Accurately and compliantly prepares and maintains documents required to be maintained internally and available for regulatory authorities and/or the sponsor prior to, during and

Clinical Research Coordinator I - Hemostasis Treatment Center jobs in United States Tags 25+ applicants Original Job Post Vanderbilt University Medical Center 0+ years exp 66 FAIR MATCH Experience Level 100 Skill 26 Industry Exp. 68 Responsibilities With assistance, prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and de

Meharry Medical College is a higher education institution focused on health sciences. They are seeking a Clinical Research Coordinator II to independently coordinate advanced clinical research projects, ensuring compliance with regulatory guidelines and institutional policies. The role involves managing study activities, maintaining records, assisting with financial functions, and supporting the Principal Investigato

AMR Clinical is hiring a Clinical Research Coordinator 1 to perform and manage tasks critical to clinical research studies. The role coordinates study activities, monitors participant safety and compliance, and supports study documentation and communication with research partners. Responsibilities Focuses on compliance responsibilities, including protocol deviations, SAE reporting, and informed consent. Strong focus