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Manager, Medical Writing

2-4 years
Not Disclosed
10 March 21, 2025
Job Description
Job Type: Full Time Education: PhD/PharmD/M.Sc 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, helping millions worldwide achieve better health. With operations in nearly 60 countries and a diverse workforce, Teva manufactures many products on the World Health Organization's Essential Medicines List. Every day, 200 million people take one of our medicines, and we are committed to finding new ways to make an impact and bring positive change.

The Opportunity:

We are seeking a Manager, Medical Writing to join our Global Regulatory Medical Writing team. The role involves writing and editing clinical regulatory documents, including submission summaries and other complex documents, while providing basic oversight, strategic assistance, and resource management for clinical research documentation.

How You’ll Spend Your Day:

  • Project-Level Work:

    • Primarily works at the project level to develop and manage clinical regulatory documents.

    • Oversees contingent workers and/or vendors as needed and provides training when required.

  • Leadership & Strategy:

    • Offers leadership and accountability by providing strategic assistance and planning support for clinical regulatory documents.

    • Ensures documents meet regulatory, departmental, and editorial standards.

  • Writing & Editing:

    • Writes and edits clinical regulatory documents, including submission summaries and other complex documents.

    • Ensures the content and context from a regulatory medical writing perspective are clear, consistent, and aligned with scientific messaging.

  • Compliance & Standards:

    • Ensures accuracy, completeness, and adherence to applicable regulatory guidelines.

    • Participates in the preparation/revision of document templates when required.

Your Experience and Qualifications:

  • Education:

    • PhD or PharmD in life sciences (or a related field) with a minimum of 2 years of experience, OR

    • Master’s degree in life sciences (or a related field) with a minimum of 4 years of experience.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities regardless of age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national origin, or any other legally protected status. We promote a diverse and inclusive workplace, ensuring that all applicants receive a fair and accessible recruitment process.