Teva Manager Medical Writing 

United States, Pennsylvania, East Bradford Township 

532410711

Join us on our journey of pivot to strategic growth:
• To make an impact, innovate, and work on diverse portfolio of products within a promising pipeline centered around our core therapeutic areas
• To help make healthcare accessible to more patients, as part of a highly global diverse matrixed R&D team,
• To improve health and enable people to live better, healthier lives.

A Manager, in Global Regulatory Medical Writing, writes and edits clinical regulatory documents, including submission summaries and other complex documents, provides basic-level oversight and guidance, as well as resource management for the direct medical-writing support in the production of clinical research documentation used in drug development and product registrations.

Travel Requirements:International and domestic

US-Based Remote (US Eastern time zone preferred)

• Write and edit clinical regulatory documents, including submission summaries and other complex documents.
• Ensure that documents include the proper content and context (from a regulatory medical writing perspective) and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
• Offer leadership and basic accountability, provide strategic assistance, and planning support for clinical regulatory documents.
• Manage contingent workers and/or vendors.
• Provide training to others as needed.

• Bachelor's degree in life sciences or related scientific discipline with at least 6 years of pharmaceutical industry regulatory writing experience. (CSRs, protocols and IBs.)

Therapy Area Head, Medical Writing

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.