Principal Medical Writer - Remote

Overview

The Principal Medical Writer at BeOne Medicines Ltd. is responsible for producing high-quality clinical and regulatory documents essential for the development and approval of oncology products.

In Short

• Develops clinical and regulatory documents including protocols and reports.
• Mentors junior medical writers.
• Manages multiple writing tasks simultaneously.
• Collaborates with study teams to ensure document quality.
• Optimizes writing processes and tools.
• Provides training and mentorship to new writers.
• Identifies risks and develops mitigation plans.
• Utilizes technical skills in Microsoft Office and document management systems.
• Participates in cross-functional process improvement.
• Fosters teamwork and provides actionable feedback.

Requirements

• MS with 4+ years or PhD/PharmD/MD with 2+ years of experience in regulatory writing.
• Advanced degree in life sciences preferred.
• Strong understanding of regulatory guidelines.
• Experience in managing complex documents.
• Excellent analytical and communication skills.
• Proficiency in Microsoft Word, Adobe Acrobat, and electronic document systems.
• Ability to work collaboratively in a team environment.
• Willingness to travel as needed.
• Experience in oncology is a plus.
• Commitment to company values of Patients First and Driving Excellence.

Benefits

• Comprehensive medical, dental, and vision plans.
• 401(k) retirement plan.
• Paid Time Off and wellness programs.
• Equity awards and stock purchase plan.
• Annual bonus plan eligibility for non-commercial roles.
• Diversity and equal opportunity workplace.
• Opportunities for professional development.
• Collaborative and innovative work environment.
• Access to a global network of professionals.
• Support for work-life balance.