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Medical Writer I - 1493

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

Medical Writer I - 1493
Date: March 21, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61246


Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and the proud producer of numerous products on the World Health Organization’s Essential Medicines List. With operations spanning nearly 60 countries and a diverse workforce, we serve millions worldwide by making healthcare more affordable and accessible. Today, at least 200 million people globally take one of our medicines daily, and we’re constantly exploring new ways to expand our positive impact.


The Opportunity:
As a Medical Writer I in the Global Regulatory Medical Writing team, you will write and edit clinical regulatory documents, including submission summaries and other complex documents. You will provide basic-level oversight, guidance, and resource management to support the production of clinical research documentation for drug development and product registrations.


How You’ll Spend Your Day:

  • Project-Level Focus: Primarily works at the project level, ensuring timely and high-quality delivery of assigned documents.

  • Vendor and Contingent Worker Management: May oversee contingent workers and vendors, and provide necessary training as needed.

  • Strategic Support: Provides leadership and basic accountability, offering strategic assistance and planning support for clinical regulatory documents.

  • Document Development: Writes and edits clinical regulatory documents, ensuring proper content, regulatory compliance, and consistent medical/scientific messaging.

  • Quality and Compliance: Ensures documents are accurate, complete, and adhere to regulatory guidelines, departmental standards, and editorial practices.

  • Template Management: 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 in medical writing, clinical research, or regulatory affairs.


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.