Vice President, Regulatory Affairs

Summit, NJ
Jul 31, 2019
Required Education
Position Type
Full time

Senior Director/VP Level

  • 10+ years pharmaceutical/biotech industry experience, PhD preferred.
  • Supervising the activities of the Regulatory Affairs team, which includes Regulatory CMC, Publishing team.
  • Developing a regulatory strategy for development programs in conjunction with the cross-functional team.
  • Ensuring content and accuracy of regulatory filings.
  • Preparing cross-functional teams for regulatory interactions.
  • Strong written and verbal communication skills with the demonstrated ability to communicate effectively and professionally.
  • Knowledge of the drug development process and global regulatory guidelines
  • Computer application skills: Advanced MS Office, Adobe Acrobat skills.

Hurley Consulting Associates offers a competitive salary, health care benefits, group life insurance, and a 401(k) plan.