IRB Operations Leader — Hybrid (Princeton)

Vitalief; Princeton (NJ); Hybrid; USD 80,000 - 100,000; Full time

Benefits offered by this job

20 PTO days

9 paid holidays

Company-paid life insurance

401(k) retirement plan

Robust healthcare options

Job summary

Vitalief is seeking an experienced IRB Operations Manager to oversee day-to-day operations of the Human Subjects Protection Program (HSPP) in Princeton, NJ. The ideal candidate will bring over 5 years of experience in human subjects research and IRB administration, ensuring compliance and effective administration.

This hybrid role includes both onsite and remote work, with robust benefits including PTO, healthcare options, and competitive compensation based on experience.

Qualifications

• 5+ years of experience in human subjects research oversight and IRB operations.
• Experience leading and supervising IRB regulatory operations.
• Strong understanding of Common Rule and FDA regulations.

Responsibilities

• Oversee day-to-day operations of the HSPP.
• Coordinate and manage IRB review processes and compliance.
• Identify operational efficiencies and support stakeholders.

Skills

Human subjects research oversight

Regulatory compliance

Leadership

Strong communication skills

Organizational skills

Education

Bachelor’s degree

Advanced degree (preferred)

Tools

Huron/eRIA or similar systems

Job description

Vitalief is seeking an experienced IRB Operations Manager to oversee day-to-day operations of the Human Subjects Protection Program (HSPP) in Princeton, NJ. The ideal candidate will bring over 5 years of experience in human subjects research and IRB administration, ensuring compliance and effective administration.

This hybrid role includes both onsite and remote work, with robust benefits including PTO, healthcare options, and competitive compensation based on experience.