Teva Senior Manager Medical Writing 

United States, Pennsylvania, East Bradford Township 

230542680

Travel Requirements:International and domestic

US-Based Remote (US Eastern time zone preferred)

• Primarily works on the product/program level
• Possible to oversee contingent workers and/or vendors; likely to provide training to others; and analyzes needs to manage resources
• Offers leadership and fundamental accountability, provides strategic supervision, and planning assistance for clinical regulatory documents
• Writes and edits clinical regulatory documents (all types).
• Ensures 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
• Participates in the preparation/revision of document templates

• Bachelor's degree in life sciences or related scientific discipline with at least 8 years of pharmaceutical industry regulatory writing experience. (CSRs, protocols and IBs.)

Therapy Area Head, Medical Writing

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