Manager, Medical Writing - Teva Pharmaceuticals - 61134
Date: March 13, 2025
Location: Bangalore, India, 560064
Who we are:
Teva Pharmaceuticals is dedicated to making good health more affordable and accessible across nearly 60 countries, impacting over 200 million people daily. As the world's leading manufacturer of generic medicines and a producer of many WHO-listed essential medicines, Teva continues to innovate and make a difference.
The opportunity:
The Manager in Global Regulatory Medical Writing is responsible for writing and editing clinical regulatory documents, including submission summaries and other complex documents. This role provides oversight and guidance in the production of clinical research documentation used for drug development and product registrations.
How you’ll spend your day:
Project-Level Work: Primarily works at the project level, ensuring timely and quality deliverables.
Vendor and Team Management: May oversee contingent workers and/or vendors and provide training as needed.
Leadership and Planning: Provides strategic assistance and planning support for clinical regulatory documents.
Medical Writing: Writes and edits clinical regulatory documents, including submission summaries and other complex documents.
Regulatory Standards: Ensures documents include proper content and context, with clear and consistent medical/scientific messaging adhering to applicable regulatory guidelines and departmental standards.
Template Preparation: May participate in the preparation and revision of document templates.
Your experience and qualifications:
Education:
PhD or PharmD in life sciences (or related field), or Master’s degree in life sciences (or related field).
Experience:
PhD or PharmD with a minimum of 2 years of experience OR Master’s degree with a minimum of 4 years of experience.
Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment regardless of legally protected statuses. We are dedicated to fostering a diverse and inclusive workplace for all.
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