Manager – Scientific Writing (Medical & Publication Writing)
Company: Teva Pharmaceuticals
Location: Bangalore, India
Employment Type: Full-Time
Function: Medical Affairs / Scientific Communications
Industry: Pharmaceuticals & Life Sciences
Experience Required: 10–12 Years
Job ID: 64974
Posting Date: December 11, 2025
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating across nearly 60 countries with a strong commitment to making quality healthcare more affordable and accessible. As one of the world’s largest producers of medicines listed on the WHO Essential Medicines List, Teva supports the health of over 200 million patients worldwide every day through innovation, science, and collaboration.
Role Overview
The Manager – Scientific Writing is responsible for delivering high-quality scientific and medical communication outputs and overseeing end-to-end publication development in compliance with Good Publication Practices (GPP) and ICMJE guidelines. This role combines strategic scientific writing, publication management, and cross-functional collaboration, translating complex clinical and scientific data into clear, impactful content for healthcare professionals, patients, and internal stakeholders.
The position requires strong therapeutic knowledge, advanced writing expertise, and experience managing global scientific communication projects within regulated pharmaceutical environments.
Key Responsibilities
Scientific & Therapeutic Expertise
Develop a strong understanding of assigned therapeutic areas and product strategies to ensure alignment with scientific communication objectives
Rapidly adapt to new therapeutic areas and support multiple portfolios concurrently
Translate complex clinical trial data and scientific concepts into clear, audience-appropriate medical content
Medical Writing & Publication Management
Author and manage core scientific deliverables, including:
Abstracts
Congress posters and presentations
Manuscripts for peer-reviewed medical journals
Collaborate with Scientific Communication Leads and Therapeutic Area experts to ensure content accuracy, relevance, and data consistency
Maintain robust document version control, traceability, and audit readiness using publication tracking systems
Adapt writing style for diverse audiences, including physicians, nurses, patients, caregivers, and internal medical teams
Monitor emerging scientific literature and assess impact on existing content
Cross-Functional Collaboration
Build and manage relationships with authors, external experts, and clinical investigators to support timely, high-quality publication development
Work closely with Medical Affairs, Clinical Development, Safety, and Regulatory teams to gather inputs and approvals
Support localization and regional adaptation of global scientific content to meet market-specific needs
Quality, Compliance & Review
Apply Good Publication Practices (GPP) and ICMJE guidelines across all scientific communication deliverables
Ensure adherence to internal SOPs, style guides, and workflows
Conduct peer reviews to maintain high scientific and editorial standards
Innovation & Continuous Improvement
Contribute to initiatives focused on improving content development processes, including the use of AI-enabled tools and structured content libraries
Support development of derivative assets such as medical affairs materials, congress toolkits, and digital scientific content
Required Experience & Qualifications
Education: Advanced degree required (PharmD, PhD, MD, or Master’s in Life Sciences or related discipline)
Experience:
10–12 years of experience in medical writing, scientific communications, or medical publications within the pharmaceutical, biotechnology, or medical device industry
Proven experience in publication writing, congress content development, and scientific literature analysis
Strong working knowledge of Good Publication Practices (GPP) and ICMJE guidelines
Familiarity with publication management systems such as Datavision, Pubstrat, Komodo, or similar platforms
Excellent written and verbal English communication skills
Strong project management, stakeholder engagement, and cross-functional collaboration abilities
Why Join Teva
Lead global scientific communication initiatives with high medical and scientific impact
Work across multiple therapeutic areas in a scientifically driven organization
Collaborate with global experts, investigators, and medical leaders
Long-term career growth in medical affairs and scientific communications
Inclusive, performance-oriented, and innovation-focused work culture
Equal Employment Opportunity
Teva Pharmaceuticals is an Equal Opportunity Employer committed to diversity and inclusion. Employment decisions are made without regard to age, race, religion, gender, disability, pregnancy, sexual orientation, gender identity or expression, national origin, or any other legally protected status. Reasonable accommodations are available throughout the recruitment process upon request.
SEO Keywords for Visibility
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