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Manager, Medical Writing

2+ years
Not Disclosed
10 April 25, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD/Pharm D 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
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61134
Date: April 11, 2025


About Teva Pharmaceuticals:
Teva Pharmaceuticals is dedicated to making good health more affordable and accessible, helping millions around the world lead healthier lives. With a global presence in nearly 60 countries, Teva is the world’s leading manufacturer of generic medicines and a proud producer of many products listed on the World Health Organization’s Essential Medicines List. At least 200 million people take Teva medicines daily, and they continue to seek innovative ways to make a positive impact on global health.


About This Role:
Teva Pharmaceuticals is seeking a Manager in Global Regulatory Medical Writing. This role involves writing and editing clinical regulatory documents, including submission summaries and other complex documents, and providing oversight and guidance for the direct medical-writing support in clinical research documentation used for drug development and product registrations. The Manager also plays a key role in resource management and strategic planning for these documents.


Key Responsibilities:

  • Document Writing and Editing:

    • Write and edit clinical regulatory documents, such as submission summaries and other complex documents.

    • Ensure that documents include the proper content, context, and clear medical/scientific messaging, adhering to regulatory guidelines and departmental standards.

  • Leadership and Oversight:

    • Oversee contingent workers and/or vendors, providing guidance and leadership as needed.

    • Provide basic accountability and strategic assistance for clinical regulatory documents.

    • Offer planning support for the preparation and revision of document templates.


Qualifications:

  • Education:

    • PhD or PharmD in life sciences or a related field, or a Master’s degree in life sciences or a 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.


Teva's Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to providing equal employment opportunities, without regard to age, race, gender, sexual orientation, disability, or any other legally recognized status entitled to protection under applicable laws. The company is dedicated to creating a diverse and inclusive workplace for all employees. If you require any accommodations during the recruitment and selection process, Teva will treat your information confidentially and use it to support an accessible candidate experience.