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 the Human Subjects Protection Program in Princeton, NJ. The role involves regulatory compliance, staff supervision, and managing IRB submissions. The ideal candidate will have extensive experience in research oversight and a strong understanding of ethical principles governing human research.

Working in a hybrid model, this full-time position offers competitive compensation, comprehensive benefits, and the chance to impact clinical research operations significantly.

Qualifications

• 5 or more years in human subjects research oversight.
• Experience in IRB regulatory operations administration.
• Strong knowledge of Common Rule and FDA regulations.
• Ability to manage IRB submissions and workflows.

Responsibilities

• Lead day-to-day operations of the HSPP.
• Oversee processing of research submissions.
• Coordinate IRB meeting activities.
• Identify operational efficiencies.

Skills

Regulatory compliance

IRB administration

Human subjects research protections

Process improvement

Analytical skills

Education

Bachelor's degree

Advanced degree preferred

Tools

Huron/eRIA

Job description

Vitalief is seeking an experienced IRB Operations Manager to oversee the Human Subjects Protection Program in Princeton, NJ. The role involves regulatory compliance, staff supervision, and managing IRB submissions. The ideal candidate will have extensive experience in research oversight and a strong understanding of ethical principles governing human research.

Working in a hybrid model, this full-time position offers competitive compensation, comprehensive benefits, and the chance to impact clinical research operations significantly.