Manager Medical Writing at Teva Pharmaceuticals, Apply Now
Teva Pharmaceuticals, a global leader in generic and specialty medicines, is seeking a Manager in medical Writing to join our team in Bangalore, India. This role offers an exciting opportunity to contribute to clinical, regulatory writing, ensuring compliance with global regulatory standards. If you have a passion for medical writing and drug development, this position will allow you to play a key role in shaping the future of healthcare.
About Teva Pharmaceuticals
With a presence in nearly 60 countries, Teva Pharmaceuticals is dedicated to improving global healthcare by making affordable and high-quality medicines accessible to millions. As the world’s largest manufacturer of generic medicines, we produce essential treatments that 200+ million people rely on daily. Our commitment to innovation, quality, and patient well-being drives us to develop life-changing therapies that enhance health outcomes worldwide.
Job Description
Job Posting: Manager, Medical Writing
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 61134
Who we are
Together, we aim to provide excellent healthcare solutions to the global community. Working with us means collaborating with a team that is dedicated to enhancing the well-being of individuals worldwide.
The Opportunity
A Manager in Global Regulatory Medical
Writing writes and edits clinical, regulatory documents, including submission summaries and other complex documents, provides basic-level oversight and guidance, as well as resource management for direct medical-writing support in the production of clinical research documentation used in drug development and product registrations.How you’ll spend your day
- Primarily works at the project level
- May oversee contingent workers and/ or vendors; may provide training to others as needed
- Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical, and regulatory documents
- Writers and edits clinical regulatory documents, including submission summaries and other complex documents
- Ensures that these documents include the proper content and context (from a regulatory medical writing perspective) and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards
- May participate in the preparation/revision of document templates
Your experience and qualifications
- PhD or PharmD in life sciences (or other related field), or Master’s degree in life sciences (or other related field)
- PhD or PharmD with a minimum of 2 years of experience OR Master’s degree with a minimum of 4 years of experience
Keywords: pharmaceuticals, medical writing, regulatory documents, drug development, healthcare solutions, Manager Medical Writing at Teva Pharmaceuticals, Apply Now
