Teva Medical Writer - 

India, Karnataka, Bengaluru 

55161292

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.

• 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
• Writers 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)

• PhD or PharmD with a minimum of 2 years of experience OR Master’s degree with a minimum of 4 years of experience