Teva Manager Medical Writing 

United States, Pennsylvania, East Bradford Township 

532410711

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

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