Manager, Medical Writing

Welcome to Teva Pharmaceutical USA, where we are dedicated to improving the lives of patients through innovative medicines and a commitment to excellence. We are currently seeking a skilled Manager of Medical Writing to join our team. As a Manager of Medical Writing, you will play a crucial role in the development and submission of high-quality regulatory documents, supporting the success of our products. We are looking for a driven and detail-oriented individual with a strong background in medical writing and a passion for delivering impactful results. If you are a self-motivated team player with excellent communication and organizational skills, we encourage you to apply for this exciting opportunity.

1. Develop and deliver high-quality regulatory documents in a timely manner to support the success of our products.
2. Collaborate with cross-functional teams to gather necessary information and ensure accuracy of content in regulatory documents.
3. Conduct thorough research and review of relevant scientific literature to support the development of regulatory documents.
4. Ensure compliance with company standards, regulations, and guidelines for the preparation of regulatory documents.
5. Manage the writing, editing, and formatting of documents, including clinical study reports, protocols, and investigator brochures.
6. Lead and mentor a team of medical writers, providing guidance and feedback to ensure consistency and quality of work.
7. Act as a subject matter expert and provide guidance on medical writing best practices to internal teams.
8. Participate in internal and external meetings to present and discuss regulatory documents, providing clarification and addressing any questions.
9. Keep up-to-date with industry and regulatory requirements and incorporate them into the development of regulatory documents.
10. Contribute to the development and implementation of standard operating procedures and templates for medical writing.
11. Maintain excellent communication and collaboration with internal and external stakeholders, including regulatory agencies.
12. Ensure all documents are produced in accordance with timelines and project priorities.
13. Review and provide feedback on documents prepared by other medical writers, ensuring accuracy and consistency.
14. Continuously evaluate and improve processes and systems to increase efficiency and quality of medical writing deliverables.
15. Adhere to all ethical, legal, and regulatory requirements in the preparation and submission of regulatory documents.

According to JobzMall, the average salary range for a Manager, Medical Writing in West Chester, PA, USA is $90,000-$110,000 per year. Salaries may vary depending on the specific company, level of experience, and other factors such as education and certifications.

Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).