Remote IRB Program Manager

Phoenix Children's; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Phoenix Children's is seeking an IRB Program Manager to supervise the development, implementation, and evaluation of clinical research trials ensuring compliance with IRB policies and federal regulations. The role coordinates resources and provides regulatory, ethical, and methodological guidance to investigators and coordinators preparing human subjects proposals.

You will oversee day-to-day IRB operations, plan training programs, develop department policies, and mentor the IRB Coordinator,

Responsibilities

• Coordinates review and approvals of research proposals by investigators through IRB and administrative procedures to ensure compliance with all requirements
• Interacts with the Office of Human Research Protections (OHRP) and Food and Drug Administration (FDA) and other governmental agencies regarding research regulations; prepares and participates (as necessary) in audits by the OHRP, FDA, or other governmental agencies
• Oversees day-to-day functions of the IRB, including pre-review of all IRB documents; generates and distributes IRB agendas, meeting packets, minutes, and correspondence in an accurate and timely manner
• Plans, develops and implements regulatory guideline training programs for physicians, coordinators and IRB members to ensure ongoing familiarity and understanding of applicable laws and requirements
• Plans, develops, implements, and evaluates all IRB department policies, procedures, and processes; implements quality assurance in conjunction with the Office of Research to ensure compliance with IRB standards and federal/state requirements
• Provides guidance to research investigators regarding FDA/OHRP requirements/regulations and IRB submission requirements
• Provides oversight and mentorship to the IRB Coordinator
• Reviews proposals and determines if they meet criteria for exemption under OHRP and FDA regulations
• Reviews proposals and determines if they meet the OHRP/FDA definition of Human Subject Research
• Reviews research study applications to ensure compliance with all federal, state, and regulatory agency requirements and specific institutional requirements; notifies appropriate individual of potentially serious adverse effects, non-compliance, and/or logistically difficult projects
• Performs miscellaneous job related duties as requested.

Job description

Phoenix Children's is seeking an IRB Program Manager to supervise the development, implementation, and evaluation of clinical research trials ensuring compliance with IRB policies and federal regulations. The role coordinates resources and provides regulatory, ethical, and methodological guidance to investigators and coordinators preparing human subjects proposals.

You will oversee day-to-day IRB operations, plan training programs, develop department policies, and mentor the IRB Coordinator,