- AbbVie (Mettawa, IL)
- …based at our Mettawa, IL location following a hybrid schedule of 3 days/week on-site. Candidates requiring remote work arrangements may be considered. ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …regulatory documents, including but not limited to: clinical study protocols, investigator brochures (IBs), clinical study reports (CSRs), and sections of regulatory ... clinical research industry, with a focus on late-stage clinical development (Phase 3 ). + Demonstrated experience in writing regulatory submission documents in … more
- Rush University Medical Center (Chicago, IL)
- …0.9 and 1.0) **Shift:** Shift 1 **Work Schedule:** 8 Hr (7:00:00 AM - 3 :00:00 PM) Rush offers exceptional rewards and benefits learn more at our Rush benefits ... of misconduct received through various means, including via Rush's confidential compliance hotline. Investigations may pertain to complaints that arise under various… more