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Senior Medical Writer

4+ years
Not Disclosed
10 April 25, 2025
Job Description
Job Type: Full Time Education: PhD/MD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Senior Medical Writer
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61563
Date: April 23, 2025


About Teva Pharmaceuticals:
Teva Pharmaceuticals is dedicated to making good health more affordable and accessible, helping millions globally lead healthier lives. As the world’s leading manufacturer of generic medicines and a proud producer of several products on the World Health Organization’s Essential Medicines List, Teva serves over 200 million people daily. The company is constantly exploring new ways to make a difference, and they welcome new people to join their mission.


About This Role:
Teva is seeking a Senior Medical Writer to support Global Regulatory Medical Writing. In this role, you will be responsible for writing and editing clinical regulatory documents, providing essential support in the production of clinical research documentation for drug development and product registrations.


Key Responsibilities:

  • Document Writing and Editing:

    • Write and edit clinical regulatory documents, including study reports, protocols, briefing books, and other submission documents (e.g., aggregate reports, post-authorization safety studies).

    • Ensure that all documents contain accurate and clear medical/scientific messaging, are complete, and adhere to regulatory guidelines and departmental standards.

  • Data Compilation and Analysis:

    • Compile, analyze, and summarize data from various sources to support document creation.

  • Quality Control:

    • Conduct proofreading, editing, document formatting, and comment resolution to maintain high document quality.

  • Leadership and Training:

    • May assist in the preparation/revision of document templates and SOPs.

    • May provide training and support to other medical writers or external vendors/contractors in document planning, processes, and content development.


Qualifications:

  • Education:

    • Bachelor's, Master's, MD, PhD, or PharmD in life sciences or related field.

  • Experience:

    • A minimum of 4+ years of relevant experience.

    • Proficiency as a lead author for protocols, aggregate reports, and clinical study reports.

    • Advanced degree is preferred.


Teva's Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to providing equal employment opportunities without regard to age, race, gender, disability, or any other legally recognized status. The company promotes a diverse and inclusive workplace and encourages applicants to request accommodations needed during the recruitment process. All accommodation information will be treated confidentially to ensure a smooth candidate experience.