Job Title:
Manager, Medical Writing
Date Posted:
3 Sept 2025
Location:
Bangalore, India, 560064
Company:
Teva Pharmaceuticals
Job ID:
63842
Company Overview:
Teva Pharmaceuticals is a global leader in generic medicines and a producer of many products on the WHO Essential Medicines List. Teva’s mission is to make healthcare more affordable and accessible, positively impacting millions of people worldwide. With operations in nearly 60 countries, Teva values diversity and inclusion, striving to innovate and improve global health outcomes.
Role Overview:
The Manager in Global Regulatory Medical Writing is responsible for authoring, editing, and overseeing clinical regulatory documents for drug development and product registrations. The role provides guidance, basic-level oversight, and resource management to support medical writing activities.
Key Responsibilities:
Write and edit clinical regulatory documents including:
Study reports
Protocols and protocol amendments
Briefing books
Investigator’s brochures
Health authority responses
Submission documents (e.g., Module 2.5 and Modules 2.7.x)
Compile, analyze, and summarize data from multiple sources.
Conduct proofreading, editing, document formatting, and comment resolution.
Ensure all documents are:
Accurate, complete, and compliant with regulatory guidelines
Consistent in medical/scientific messaging
Adherent to departmental and editorial standards
Participate in preparing or revising document templates and SOPs.
Train and support medical writers or external vendors/contractors on document planning, processes, and content development.
Required Qualifications:
Bachelor’s, Master’s, MD, PhD, or PharmD in life sciences or related field (advanced degree preferred).
Minimum of 5+ years of relevant experience (6+ years for advanced degree holders).
Proficient as lead author for:
Protocols and protocol amendments
Clinical study reports
Investigator’s brochures
Clinical summary documents (Modules 2.5 and 2.7.1–2.7.4)
Up to 10% travel may be required.
Skills & Competencies:
Strong scientific and regulatory writing skills.
Attention to detail and ability to ensure consistency in medical/scientific content.
Ability to manage resources, provide guidance, and train team members.
Effective communication and collaboration skills.
Equal Opportunity Statement:
Teva Pharmaceuticals is committed to equal opportunity in employment. Employment decisions are based on merit, qualifications, and business requirements without regard to age, race, religion, sex, disability, sexual orientation, gender identity, or other legally protected status. Reasonable accommodations are provided to support candidates during the recruitment process.
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