IRB Program Manager ! Clinical Research Admin Telecommuting Quick ! Clinical

Department: RSRCH-GRNT | Clinical Research Admin

Location:

Telecommuting

Shift: Mon-Fri, Days, 8am-5pm

Category:
Research

Posting #: 1066705

Employee Type:
Full-Time

This position supervises the development, implementation, and evaluation of clinical research trials to ensure consistency with all IRB policies and procedures; coordinates resource requirement and utilization to ensure compliance with required federal, state, funding source, and all other applicable governing regulations, requirements, and standards. This position also provides regulatory, ethical and methodological guidance to investigators and coordinators to prepare applications for research proposals involving human subjects and provides consultation to IRB members and institutional officials regarding federal regulations and institutional policy.

• 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.

Mission

To advance hope, healing and the best healthcare for children and their families

Vision

Phoenix Children's will be the leading pediatric health system in the Southwest, nationally recognized for exceptional care, innovative research and advanced medical education.

We realize this vision by:

• Offering the most comprehensive care across ages, communities and specialties
• Investing in innovative research, including emerging treatments, tools and technologies
• Advancing education and training to shape the next generation of clinical leaders
• Advocating for the health and well-being of children and families

Values

• We place children and families at the center of all we do
• We deliver exceptional care, every day and in every way
• We collaborate with colleagues, partners and communities to amplify our impact
• We set the standards of pediatric healthcare today, and innovate for the future
• We are accountable for making the highest quality care accessible and affordable

Please review the following qualifications and specify whether you meet each of the requirements listed.

Do you meet this requirement or have the ability to obtain it within the timeframe listed in the requirement? 1. Bachelors degree in a related field

Preferred

Do you meet this requirement or have the ability to obtain it within the timeframe listed in the requirement? 1. Four (4) or more years of experience in human research protection administration

Required

2. Experience with applicable federal and state guidelines and regulations

Preferred

3. Four (4) or more years of experience as an IRB Coordinator

Preferred

Do you meet this requirement or have the ability to obtain it within the timeframe listed in the requirement? 1. Certification in IRB Management (CIM) or Certified IRB Professional (CIP) OR…