Associate Director, Clinical Development Medical Writing (Remote)

Exciting Opportunity: Manager, Global Regulatory Medical Writing

Location: US-Based Remote (Eastern Time Zone preferred)

About the Role: Join us as a Manager in Global Regulatory Medical Writing, where you'll play a crucial role in shaping drug development and product registrations. You'll write and edit critical clinical regulatory documents, ensuring compliance with regulatory guidelines and maintaining high standards of accuracy and completeness.

Your Day-to-Day:

· Write and edit clinical regulatory documents, including submission summaries and other complex documents.

· Provide leadership and basic oversight for medical-writing support in the production of clinical research documentation.

· Ensure documents adhere to regulatory guidelines and departmental standards.

· Manage contingent workers and/or vendors, providing training as needed.

Your Experience and Qualifications:

· Bachelor's degree in life sciences or related field.

· Minimum 6 years' pharmaceutical industry regulatory writing experience.

Why Join Us: In addition to a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage, we offer opportunities for growth and development. Join us and be part of a team shaping the future of pharmaceuticals.