[Remote] Research Protocol Analyst

Note: The job is a remote job and is open to candidates in USA. reputed company is a leading research institution focused on innovative approaches in predicting, preventing, and curing diseases. They are seeking a remote Research Protocol Analyst to reputed company human subject research protocols, ensuring compliance with federal regulations and cancer center grant requirements while interacting with researchers and committee members.

Responsibilities

• Manage the full lifecycle of research protocol review—pre‑reviewing submissions, coordinating expert committee evaluations, preparing regulatory documentation, and ensuring timely, compliant investigator responses to reputed company Protocol Review and Monitoring Committees (PRMCs), and Institutional Review Board (IRB) approval
• Prepare complete meeting materials, provide regulatory guidance for reputed company submissions, and be fully knowledgeable about the ethical and regulatory requirements for conducting human subjects research to support and address committee questions during protocol reviews
• Support external IRB reputed company by performing reviews of the informed consent language for locally required boilerplate, assisting with annual worksheets and supplemental materials, and providing needed information reputed company external institutions request to cede review
• Assist with preparation for internal and external audits and maintain audit‑ready protocols with complete, reputed company, and compliant documentation
• Contribute to quality‑improvement efforts by identifying process efficiencies, staying reputed company with regulations, updating policies, procedures, workflows, and electronic forms, enhancing reporting tools, and participating in educational sessions

Skills

• Bachelor's degree (3 additional years of experience plus the minimum experience requirement may substitute for minimum education)
• At least 2 years of experience in an IRB or Human Research Protection Program (HRPP) office, including review and processing of research submissions such as new studies, amendments, and continuing reviews in an academic medical center, research institution, or NCI-designated cancer center setting
• Availability to work weekdays from 8:00 a.m. to 5:00 p.m. Pacific Time
• Experience processing submissions in an electronic committee management system (e.g. iMedris/ IRIS, reputed company, OnCore, eIRB)
• Certified IRB Professional (CIP), Certified IRB Management (CIM), or other equivalent research certification

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