Manager – Scientific Writing
Company: Teva Pharmaceuticals
Location: Bangalore, India (560064)
Employment Type: Full-time
Experience Required: 10–12 Years
Job ID: 64974
Posted Date: December 11, 2025
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating in nearly 60 countries. With a strong commitment to improving access to affordable, high-quality healthcare, Teva supports millions of patients worldwide every day. The organization’s diverse and inclusive workforce is united by a mission to deliver impactful scientific and medical solutions that improve lives globally.
Role Overview
Teva is seeking an experienced Manager – Scientific Writing to lead and deliver high-quality scientific and medical communication projects in compliance with global publication standards. This role is responsible for developing and managing scientific content for peer-reviewed journals, congress submissions, abstracts, posters, and presentations, ensuring accuracy, clarity, and alignment with evolving clinical data.
The position requires deep scientific expertise, strong leadership and project management capabilities, and the ability to translate complex clinical and regulatory information into clear, audience-appropriate scientific narratives for healthcare professionals, patients, and internal stakeholders.
Key Responsibilities
Scientific & Therapeutic Expertise
Develop a strong understanding of assigned therapeutic areas and product strategies to support scientific communication objectives
Rapidly adapt to new therapeutic areas and manage content across multiple disease areas
Translate complex clinical trial data and scientific evidence into clear, accurate, and impactful content
Medical Writing & Publication Management
Author and oversee development of abstracts, congress posters and presentations, and manuscripts for peer-reviewed medical journals
Partner with Scientific Communication Leads and Therapeutic Area Leads to ensure global scientific content remains current, compliant, and aligned with emerging data
Maintain robust version control, documentation, and audit-ready records using Teva’s publication tracking tools
Adapt scientific writing style for diverse audiences, including specialist HCPs, nurses, patients, caregivers, and other stakeholders
Monitor scientific literature and emerging publications to assess impact on existing materials and update content as required
Cross-Functional Collaboration
Build and maintain effective relationships with authors, external experts, and clinical investigators to enable timely, high-quality publications
Collaborate closely with Medical Affairs, Clinical Development, Safety, Regulatory, and external partners to secure reviews and approvals
Support localization and adaptation of global scientific content to meet regional regulatory, cultural, and market-specific requirements
Quality, Compliance & Review
Apply Good Publication Practices, including ICMJE Guidelines, across all scientific communication deliverables
Ensure strict adherence to internal SOPs, style guides, and standardized workflows
Conduct peer reviews and provide mentoring feedback to maintain high-quality scientific writing standards
Innovation & Continuous Improvement
Contribute to process optimization initiatives, including use of AI-enabled authoring tools, structured content libraries, and digital asset management systems
Support creation of derivative scientific assets, including field medical materials, congress support content, and digital communication tools
Qualifications & Experience
Education
Advanced degree required: PharmD, PhD, MD, or Master’s degree in Life Sciences or a related discipline
Professional Experience
10–12 years of experience in medical writing, scientific communications, or medical information within the pharmaceutical, biotechnology, or medical device industry
Proven experience in publication writing, congress material development, and scientific literature evaluation
Strong working knowledge of Good Publication Practices and ICMJE Guidelines
Hands-on experience with publication management systems such as Datavision, Pubstrat, Komodo, or similar platforms
Language Skills
Professional-level proficiency in written and spoken English
Why Join Teva
Work with a globally recognized pharmaceutical leader
Contribute to impactful scientific communications that improve patient outcomes worldwide
Collaborate with cross-functional and international teams
Be part of a diverse, inclusive, and innovation-driven work environment
Equal Employment Opportunity
Teva Pharmaceuticals is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, religion, gender, disability, sexual orientation, gender identity or expression, veteran status, or any other protected status under applicable laws. Reasonable accommodations are available throughout the recruitment process to support an accessible candidate experience.
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