Job Title: Manager, Medical Writing
Date Posted: Sep 3, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 63842
Company Overview:
Teva Pharmaceuticals is dedicated to making health more affordable and accessible worldwide. With operations in nearly 60 countries and a diverse workforce, Teva is the world’s leading manufacturer of generic medicines and the producer of many products on the WHO Essential Medicines List. Today, more than 200 million people take Teva medicines daily.
Opportunity Overview:
The Manager, Global Regulatory Medical Writing is responsible for writing and editing clinical regulatory documents including submission summaries and other complex documents. The role provides basic oversight, guidance, and resource management for medical writing support in producing documentation essential for drug development and product registrations.
Key Responsibilities:
Document Development
Write and edit clinical regulatory documents: study reports, protocols, briefing books, investigator’s brochures, health authority responses, and 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 documents are accurate, complete, scientifically sound, and compliant with regulatory guidelines and departmental standards.
Quality & Compliance
Ensure consistency in regulatory medical writing content and scientific messaging.
Maintain adherence to internal SOPs, templates, and editorial standards.
Process & Oversight
Participate in the development/revision of document templates and SOPs.
Provide oversight and guidance to writers, vendors, or contractors on document planning, processes, and content.
May train and mentor medical writers to improve quality and efficiency.
Experience & Qualifications:
Education:
Bachelor’s, Master’s, MD, PhD, or PharmD in Life Sciences (or related field).
Advanced degree preferred (Master’s, MD, PhD, or PharmD).
Experience:
University degree with 5+ years of relevant medical writing experience (advanced degree preferred).
6+ years with an advanced degree.
Demonstrated proficiency as a lead author in writing:
Protocols/protocol amendments
Clinical study reports
Investigator’s brochures
Clinical summary documents (Modules 2.5, 2.7.1–2.7.4)
Other Requirements:
Travel: up to 10%
Equal Employment Opportunity:
Teva Pharmaceuticals is an equal opportunity employer. Employment is provided without regard to race, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity, veteran status, national origin, or any other legally protected status. Accommodations are available during the recruitment and selection process upon request.
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