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Teva Senior Manager Medical Writer 
United States, Pennsylvania, East Bradford Township 


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.

How you’ll spend your day
  • 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.
Your experience and qualifications
  • 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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