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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 / Entry-Level Opportunity)

Location: Bangalore, India – 560064
Category: Medical Writing / Scientific Communication / Pharmaceutical Publications
Job Type: Full-Time
Experience Required: Fresher / 0–2 Years
Job ID: 64974


Company Overview

Teva Pharmaceuticals is a global leader in the pharmaceutical industry, committed to improving access to affordable healthcare. With operations in nearly 60 countries, Teva develops both generic and specialty medicines that improve the lives of over 200 million patients worldwide.

This position offers freshers an opportunity to begin a rewarding career in scientific writing, medical communications, and pharmaceutical publications, working alongside experienced professionals in a global environment.


Role Overview

The Manager – Scientific Writing will support high-quality medical writing and project management of scientific communication deliverables. This includes abstracts, posters, congress presentations, and manuscripts for peer-reviewed journals.

The role requires strong scientific knowledge, excellent writing skills, and the ability to translate complex clinical and scientific data into clear, accessible content for healthcare professionals (HCPs), patients, and other stakeholders.


Key Responsibilities

Scientific Knowledge & Communication

  • Quickly understand therapeutic areas and product strategies to support scientific communication goals.

  • Translate complex clinical data into content suitable for diverse audiences, including HCPs and patients.

  • Monitor scientific literature to ensure content remains accurate and current.

Medical Writing & Publication Management

  • Assist in drafting scientific communication deliverables, including abstracts, posters, presentations, and manuscripts.

  • Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure content alignment with global strategies.

  • Maintain robust version control and document tracking for transparency, audit-readiness, and traceability.

  • Adapt writing style for specialist HCPs, patients, nurses, caregivers, and other stakeholders.

Collaboration & Review

  • Coordinate with authors, clinical investigators, and external experts to ensure high-quality deliverables.

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

  • Support adaptation of global content to meet regional or market-specific regulatory and cultural requirements.

Quality & Compliance

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

  • Follow SOPs, style guides, and internal workflows to ensure consistent and compliant outputs.

  • Conduct peer reviews to uphold quality standards.

Innovation & Continuous Improvement

  • Participate in initiatives to improve content development processes using AI tools, structured content libraries, and digital asset management systems.

  • Support creation of derivative content, including field medical affairs materials, congress materials, and digital assets.


Qualifications & Skills

Education:

  • Advanced degree (PharmD, PhD, MD, or Master’s in Life Sciences or related field) preferred. Fresh graduates with strong academic performance are encouraged to apply.

Experience:

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

  • Exposure to clinical data interpretation, scientific literature, or content development is a plus.

Skills:

  • Excellent professional English communication (written and verbal).

  • Strong scientific knowledge and analytical skills.

  • Familiarity with publication management systems (Datavision, Pubstrat, Komodo) is advantageous.

  • Detail-oriented, organized, and able to manage multiple tasks efficiently.

  • Ability to work collaboratively in cross-functional teams.


Why Join Teva?

  • Launch a career in scientific writing and medical communications within a global pharmaceutical leader.

  • Gain hands-on experience in publication development, congress content preparation, and regulatory-compliant medical writing.

  • Work with industry experts and develop skills for medical writing, medical affairs, and pharmaceutical communication careers.


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. Accommodations will be provided for candidates needing support during the recruitment process.