IRB Program Manager

National Medical Association; Phoenix (AZ); Remote; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking organization dedicated to advancing clinical research. This role offers the opportunity to supervise the development and evaluation of clinical research trials, ensuring adherence to ethical standards and regulatory compliance. With a focus on providing guidance to investigators and IRB members, you will play a crucial role in shaping research involving human subjects. This position is ideal for a professional with a strong background in human research protection and a passion for maintaining high ethical standards in research practices. Flexible remote work options are available, making this a fantastic opportunity for those seeking a balanced work environment.

Qualifications

• 4+ years of experience in human research protection administration.
• Certification in IRB Management or Certified IRB Professional required.

Responsibilities

• Supervise clinical research trials to ensure compliance with regulations.
• Provide guidance to investigators for research proposals involving human subjects.

Skills

Human Research Protection Administration

Regulatory Compliance

Ethical Guidance

Methodological Guidance

Education

Bachelor's Degree in a Related Field

Job description

Position Summary

Remote available in most states.

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.

Education

• Bachelors degree in a related field (Preferred)

Experience

• Four (4) or more years of experience in human research protection administration (Required)
• Experience with applicable federal and state guidelines and regulations (Preferred)
• Four (4) or more years of experience as an IRB Coordinator (Preferred)

Certifications

• Certification in IRB Management (CIM) or Certified IRB Professional (CIP) OR qualified to sit for exam and pass exam prior to employment start date (Required)