Jersey City, New Jersey
•
Yesterday
Job Title: Regulatory Studio CMS Senior ManagerLocation: 100% Onsite New Brunswick (preferred) or Lawrenceville, NJDuration: 11 Months Contract Top Required Skills / Must-Haves: 2 3 years of Small Molecule Drug Development experienceHands-on experience with Veeva System (Documentum)Strong verbal and written communication skills5+ years in the pharmaceutical industry3+ years CMC regulatory experience (Sterile Injectable experience preferred) The highlights are as below: - Experience with Veeva
Easy Apply
Full-time
Depends on Experience