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Global Clinical Documentation Lead

1 week ago


Parsippany, New Jersey, United States Tevapharm Full time

Pursue a career with a company committed to equal opportunity in employment, dedicated to making a difference in the lives of millions around the world. We're seeking an experienced Senior Director to join our team in Global Regulatory Medical Writing & Data Transparency.

About the Role

In this position, you'll lead a team of medical writers/managers and electronic document specialists within Clinical Specialty Development. Your focus will be on producing high-quality clinical research documentation, ensuring adherence to departmental standards and regulatory guidelines.

Your key responsibilities will include:

  • Providing leadership, direction, and competence to a global team.
  • Liaising among internal/global functional groups to optimize resource utilization.
  • Mentoring manager-level direct reports.

This is a unique opportunity to work in a dynamic environment, shaping the future of healthcare and contributing to the success of our organization.