Instagram
youtube
Facebook

Manager, Medical Writing

5+ years
Not Disclosed
10 Sept. 22, 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

Job Title:

Manager, Medical Writing

Date Posted:

3 Sept 2025

Location:

Bangalore, India, 560064

Company:

Teva Pharmaceuticals

Job ID:

63842


Company Overview:

Teva Pharmaceuticals is a global leader in generic medicines and a producer of many products on the WHO Essential Medicines List. Teva’s mission is to make healthcare more affordable and accessible, positively impacting millions of people worldwide. With operations in nearly 60 countries, Teva values diversity and inclusion, striving to innovate and improve global health outcomes.


Role Overview:

The Manager in Global Regulatory Medical Writing is responsible for authoring, editing, and overseeing clinical regulatory documents for drug development and product registrations. The role provides guidance, basic-level oversight, and resource management to support medical writing activities.


Key Responsibilities:

  • Write and edit clinical regulatory documents including:

    • Study reports

    • Protocols and protocol amendments

    • Briefing books

    • Investigator’s brochures

    • Health authority responses

    • Submission documents (e.g., Module 2.5 and Modules 2.7.x)

  • Compile, analyze, and summarize data from multiple sources.

  • Conduct proofreading, editing, document formatting, and comment resolution.

  • Ensure all documents are:

    • Accurate, complete, and compliant with regulatory guidelines

    • Consistent in medical/scientific messaging

    • Adherent to departmental and editorial standards

  • Participate in preparing or revising document templates and SOPs.

  • Train and support medical writers or external vendors/contractors on document planning, processes, and content development.


Required Qualifications:

  • Bachelor’s, Master’s, MD, PhD, or PharmD in life sciences or related field (advanced degree preferred).

  • Minimum of 5+ years of relevant experience (6+ years for advanced degree holders).

  • Proficient as lead author for:

    • Protocols and protocol amendments

    • Clinical study reports

    • Investigator’s brochures

    • Clinical summary documents (Modules 2.5 and 2.7.1–2.7.4)

  • Up to 10% travel may be required.


Skills & Competencies:

  • Strong scientific and regulatory writing skills.

  • Attention to detail and ability to ensure consistency in medical/scientific content.

  • Ability to manage resources, provide guidance, and train team members.

  • Effective communication and collaboration skills.


Equal Opportunity Statement:

Teva Pharmaceuticals is committed to equal opportunity in employment. Employment decisions are based on merit, qualifications, and business requirements without regard to age, race, religion, sex, disability, sexual orientation, gender identity, or other legally protected status. Reasonable accommodations are provided to support candidates during the recruitment process.