Research Misconduct Investigations Analyst

About Vitalief Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care.

We bring deep clinical research expertise together with practical, results-driven consulting to help organizations operate more efficiently and achieve sustainable growth.

The Role We are seeking an experienced Research Misconduct Investigations Analyst that will support our client’s (a clinical research academic university) commitment to research integrity by assisting in the assessment, inquiry, and investigation of allegations of research misconduct.

The Analyst coordinates investigative activities, manages confidential records, and ensures adherence to federal, state, and institutional regulations.

This role works closely with the Office of General Counsel to prepare communications and regulatory reports for federal oversight agencies.

Engagement Details Work Hours :

• 20 to 30 hours per week Contract Duration : 6 months  (possible extension) Pay Rate : Market competitive (depends on experience level) Location : Must be available for two initial weeks of on-site training in Piscataway, NJ (at your own expense), then the role is 100% remote after the training period .

Key Responsibilities :

Required Qualifications :

Preferred Qualifications :

PHYSICAL DEMANDS :