Teva Pharmaceuticals Hiring Medical Writing Associate

career journey with Teva Pharmaceuticals! We are thrilled to announce an exciting opportunity for a Medical Writing Associate I to join dynamic team in Bangalore, India (560064). At Teva Pharmaceuticals, committed to making good health more affordable and accessible globally. If you’re passionate about contributing to the well-being of millions worldwide, this role might be your perfect fit.
About Teva Pharmaceuticals:
- Company Name: Teva Pharmaceuticals
- Location: Bangalore, India, 560064
- Job ID: 53122
Join us on our mission to make good health accessible to millions around the world. Teva Pharmaceuticals operates in nearly 60 countries, fostering a diverse and inclusive workplace. As the world’s leading manufacturer of generic medicines, we take pride in producing many of the products listed on the World Health Organization’s Essential Medicines List. Every day, at least 200 million people globally trust and benefit from our medicines. Be a part of our journey and help us make an even greater impact.
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Position Title | Medical Writing Associate I |
---|---|
Job ID | 53122 |
Company | Teva Pharmaceuticals |
Location | Bangalore, India, 560064 |
Job Description:
As a Medical Writing Associate I at Teva Pharmaceuticals, you will:
- Conduct literature searches and prepare clinical study protocols and Patient Support Programs (PSP) in compliance with guidelines and regulatory requirements.
- Prepare Informed Consent Forms (ICF) aligned with clinical study protocols.
- Perform MedDRA and WHO-DD coding of clinical studies.
- Review and prepare Case Record Forms (CRF).
- Contribute to system improvements.
- Prepare Clinical Study Reports.
About the Department & Responsibilities:
This role reports to the Project Manager IV in R&D Project/Program Management.
Your Experience and Qualifications:
- Educational Background: M.Pharm (Pharmacology)
- Experience: 1-2 years in protocol writing
Employment Details:
- Role Category: Medical Writing Associate I
- Employment Type: Full-Time
- Reports To: Project Manager IV R&D Project/Program Management
Key Skills: Medical Writing, Pharmacology, Clinical Study Protocols, ICF, CRF, MedDRA, WHO-DD Coding.
Apply online

To apply for this job please visit careers.teva.
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