Job Title:
Manager, Medical Writing
Location:
Bangalore, India – 560064
Company:
Teva Pharmaceuticals
Job ID:
63842
Posting Date:
September 3, 2025
Company Overview:
Teva Pharmaceuticals is a global leader in generic medicines and a proud producer of many products on the World Health Organization’s Essential Medicines List. Teva is committed to making good health more affordable and accessible, impacting millions of lives worldwide.
Role Summary:
The Manager in Global Regulatory Medical Writing is responsible for writing and editing clinical regulatory documents, providing oversight, guidance, and resource management for medical writing activities supporting clinical research and regulatory submissions.
Key Responsibilities:
Document Preparation & Editing
Write and edit clinical regulatory documents, including:
Study reports, protocols, briefing books, investigator’s brochures
Submission documents (e.g., Module 2.5 and Modules 2.7.x)
Compile, analyze, and summarize data from multiple sources.
Conduct proofreading, formatting, and comment resolution.
Ensure documents are accurate, complete, and follow regulatory guidelines.
Quality & Compliance
Ensure clear and consistent medical/scientific messaging.
Maintain adherence to departmental standards and editorial requirements.
Support the preparation or revision of document templates and SOPs.
Leadership & Mentorship
Provide guidance to medical writers and/or external vendors/contractors.
Train team members on document planning, process adherence, and content development.
Project Management
Manage medical writing resources at the project level.
Coordinate timelines and deliverables for assigned documentation.
Qualifications & Experience:
Education:
Bachelor’s, Master’s, MD, PhD, or PharmD in life sciences or related field.
Advanced degree preferred (Master’s, MD, PhD, PharmD).
Experience:
Minimum 5+ years of relevant medical writing experience with Bachelor’s degree; 6+ years with advanced degree.
Proven experience as lead author on:
Protocols and protocol amendments
Clinical study reports
Investigator’s brochures
Clinical summary documents (modules 2.5, 2.7.1–2.7.4)
Skills:
Strong analytical and scientific writing skills.
Attention to detail and adherence to regulatory standards.
Ability to manage multiple projects and coordinate with cross-functional teams.
Travel:
Up to 10%
Equal Opportunity Statement:
Teva Pharmaceuticals is committed to providing equal employment opportunities without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status. Teva fosters a diverse and inclusive workplace. Accommodations are provided for candidates throughout the recruitment process as needed.
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