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Manager, Medical Writing

4+ years
Not Disclosed
10 March 26, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD/PharmD 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, Medical Writing
Date: March 13, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61134


Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and a key contributor to the World Health Organization’s Essential Medicines List. Operating across nearly 60 countries with a diverse workforce, we strive to make healthcare affordable and accessible, helping millions worldwide enjoy healthier lives. With 200 million people using our medicines daily, we are constantly seeking innovative ways to expand our impact and welcome new talent to contribute to this mission.


The Opportunity:
The Manager, Global Regulatory Medical Writing is responsible for writing and editing clinical regulatory documents, including submission summaries and other complex documents. The role involves providing basic-level oversight, guidance, and resource management for direct medical writing support used in clinical research documentation, aiding drug development and product registrations.


How You’ll Spend Your Day:

  • Project-Level Focus: Primarily works at the project level, managing writing assignments and document deliverables.

  • Oversight and Training: May oversee contingent workers and/or vendors while providing training as needed.

  • Leadership and Planning Support: Offers leadership, strategic assistance, and planning support for clinical regulatory documents.

  • Writing and Editing: Writes and edits clinical regulatory documents, ensuring accuracy, clarity, and adherence to regulatory and editorial standards.

  • Regulatory Compliance: Ensures documents include the correct content, context, and medical/scientific messaging while complying with applicable regulatory guidelines.

  • Template Development: May participate in the preparation and revision of document templates.


Your Experience and Qualifications:

  • Education:

    • PhD or PharmD in Life Sciences or related field, or

    • Master’s degree in Life Sciences or related field.

  • Experience:

    • PhD or PharmD with a minimum of 2 years of experience, OR

    • Master’s degree with a minimum of 4 years of experience.


Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure that all qualified applicants are considered without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status.

If you are contacted for a job opportunity, please inform us of any accommodations needed to facilitate an inclusive and accessible candidate experience.