All jobs → Partner boards

Regulatory Specialist

University of Minnesota • Minneapolis, MN, US • published 2026-09-29 08:55:30.955141

Description

All required qualifications must be documented on application materials. REQUIRED QUALIFICATIONS * BA/BS and minimum of 4 year of clinical research or related experience or advanced degree plus 2 year of experience * Experience with clinical research trials regulations (e.g., Food and Drug Administration (FDA) and Good Clinical Practice (GCP)). * Experience submitting materials to IRB and with following policies and procedures. * Knowledge of basic anatomy and medical terminology * Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment * Strong written and verbal communication skills, including computer proficiency in a PC environment with Microsoft Office products. Preferred * Certified Clinical Research Professional (or similar) certification * Experience in oncology clinical research setting * Previous professional experience on a clinical research project team or similar environment * Experience writing and adapting patient consent forms for research studies * Experience using UMN health sciences software and document management systems (e.g., OnCore, Florence eBinders, Smartsheet, varyi...

Get jobs like this daily in Telegram: @careeri_bot