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Mgr Scientific Writing

0-2 years
Not Disclosed
10 Nov. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 (Fresher / Early-Career Opportunity)

Location: Bangalore, India – 560064
Category: Scientific Writing / Medical Communications / Pharma Publications
Job Type: Full-Time
Experience Required: Fresher / 0–2 Years
Job ID: 64972


Company Overview

Teva Pharmaceuticals is a leading global pharmaceutical company dedicated to making healthcare more accessible and affordable. Operating in nearly 60 countries, Teva produces medicines that improve the lives of over 200 million patients worldwide. As a pioneer in generic and specialty medicines, Teva is committed to scientific excellence, compliance, and innovation.

This position provides an excellent opportunity for freshers and early-career professionals to start a career in scientific writing and medical communications, gaining exposure to global pharmaceutical publications and congress content.


Role Overview

As a Manager – Scientific Writing, you will contribute to the development of high-quality scientific communication deliverables, including abstracts, posters, presentations, and manuscripts for peer-reviewed journals and congresses. You will support internal and external stakeholders by translating complex clinical data into clear, accurate, and accessible content for healthcare professionals (HCPs), patients, and other audiences.

This role combines scientific expertise, communication skills, and compliance knowledge, offering exposure to end-to-end publication processes and medical writing workflows.


Key Responsibilities

Scientific Knowledge & Communication

  • Quickly understand therapeutic areas and product strategies to align scientific communication objectives.

  • Translate complex clinical and scientific information into clear content for diverse audiences, including HCPs, patients, caregivers, and other stakeholders.

  • Monitor scientific literature and emerging publications to update content and ensure accuracy.

Medical Writing & Publication Management

  • Assist in writing key deliverables: abstracts, posters/presentations, manuscripts, and other scientific materials.

  • Support collaboration with Scientific Communication Leads and Therapeutic Area Leads to ensure content is current and relevant.

  • Maintain version control and documentation to ensure transparency, traceability, and audit readiness.

  • Adapt writing style to meet audience and regulatory requirements.

Collaboration & Review

  • Work with authors, clinical trial investigators, and external experts to facilitate high-quality publications.

  • Collaborate cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams.

  • Support localization of global content to meet regional and market-specific needs.

Quality & Compliance

  • Apply Good Publication Practices (GPP) and ICMJE Guidelines in all deliverables.

  • Follow internal SOPs, style guides, and workflows to ensure consistency and compliance.

  • Conduct peer reviews and quality checks of content produced by others.

Innovation & Continuous Improvement

  • Participate in initiatives to improve content development processes.

  • Support derivative content development, including congress preparation materials and digital assets.


Qualifications & Skills

Education:

  • Advanced degree (PharmD, PhD, MD, or Master’s in Life Sciences or related field) preferred, but fresh graduates are welcome with strong academic performance.

Experience:

  • Fresher / 0–2 years in scientific writing, medical communications, or pharma publications.

  • Exposure to medical writing projects, clinical literature analysis, or scientific documentation is a plus.

Skills:

  • Excellent written and oral English communication skills.

  • Strong scientific understanding and ability to interpret clinical trial data.

  • Basic knowledge of publication management systems and workflows (e.g., Datavision, Pubstrat, Komodo).

  • Ability to work collaboratively in cross-functional teams.

  • Detail-oriented, organized, and capable of managing multiple tasks.


Why Join Teva?

  • Launch your career in scientific writing and medical communications in a global pharmaceutical company.

  • Gain hands-on exposure to publication development, congress content preparation, and regulatory-compliant writing.

  • Work alongside industry experts in a collaborative, innovative environment.

  • Develop professional skills that advance your career in medical writing, medical affairs, and pharma communications.


Equal Employment Opportunity

Teva Pharmaceuticals is committed to a diverse and inclusive workplace. Employment decisions are made without regard to age, race, color, religion, sex, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Accommodation will be provided for candidates needing support during the recruitment process.


Apply Now: Start your career in Scientific Writing – Pharmaceutical Industry with Teva Pharmaceuticals, and gain hands-on experience in global medical communications, publication management, and clinical data translation.