Teva Senior Manager Medical Writer 

United States, Pennsylvania, East Bradford Township 

202535974

A Senior 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.

• Primarily works at project level.
• May oversee contingent workers and/ or vendors; may provide training to others as needed.
• Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents.
• Writes and edits clinical regulatory documents, including submission summaries and other complex documents.
• Ensures that these 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.
• May participate in the preparation/revision of document templates.

• PhD or PharmD in life sciences (or other related field), or Master’s degree in life sciences (or other related field). Or, PhD or PharmD with a minimum of 2 years of experience or Master’s degree with a minimum of 6 years of experience.
• Specialized or Technical Knowledge Licenses, Certifications needed: Mastery of Microsoft (MS) Word.

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