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Mgr Scientific Writing

Teva Pharmaceuticals
Teva Pharmaceuticals
10-12 years
preferred by company
10 Dec. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.


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