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Medical Writer I - 1493

2+ years
Not Disclosed
10 April 25, 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
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61246
Date: April 22, 2025


About Teva Pharmaceuticals:
Teva Pharmaceuticals is on a mission to make good health more affordable and accessible, helping millions around the world lead healthier lives. With a 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. Today, at least 200 million people take Teva medicines daily. The company continues to strive to make a difference and is always seeking new ways and new people to help fulfill this mission.


About This Role:
Teva Pharmaceuticals is looking for a Medical Writer I in Global Regulatory Medical Writing. This position involves writing and editing clinical regulatory documents, such as study reports, protocols, briefing books, and other submission documents. The role is focused on providing support in the production of clinical research documentation used in drug development and product registrations.


Key Responsibilities:

  • Document Writing and Editing:

    • Write and edit clinical regulatory documents including study reports, protocols, and other submission documents.

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

  • Quality Control:

    • Conduct proofreading, editing, document formatting, and comment resolution.

    • Ensure documents include proper content and context from a regulatory medical writing perspective.

  • Collaboration and Support:

    • May assist in training and supporting other medical writers or external vendors in document planning, processes, and content development.


Qualifications:

  • Education:

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

  • Experience:

    • PhD or PharmD with at least 2 years of experience, or a Master’s degree with at least 4 years of experience in regulatory 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. The company strives to maintain a diverse and inclusive workplace for all. If you are contacted for a job opportunity, Teva will make accommodations as needed to support you throughout the recruitment and selection process. All accommodation information will be treated confidentially to ensure an accessible candidate experience.