Job Summary

• This role will lead the preparation of clinical study synopses, minutes for clinical development advisory boards and steering committees, and clinical sections of regulatory documents in close collaboration with the Global Clinical Leads, Global Clinical Operations, biostatisticians, and other cross-functional colleagues.
• The Senior Medical Writer will identify, engage, and manage the work of contract medical writers as required.
• At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity.

Matching Summary

Skills & Requirements

Key Requirements

• Master’s degree in a scientific or related field
• 8+ years’ experience in regulatory writing
• Experience overseeing and mentoring contractors
• Strong understanding of drug development
• Proficiency with document templates and version control

Work Rights