Medical Writer

Job Description

Join Telix Pharmaceuticals as a Medical Writer and contribute to our strategic goals by leading the writing process for clinical drug development. You will plan and prepare clinical and regulatory documents, organize and interpret scientific and statistical data, and compile high-quality reports. Collaborate with colleagues to respond to health authority requests, develop SOPs, and maintain expertise in medical writing.

Qualifications

1. Bachelor's degree in science or related field; advanced degree preferred. 2. 5+ years of experience in regulatory medical writing. 3. Strong understanding of drug development, regulations (CFR, FDA, EMA, and ICH guidelines), and scientific principles. 4. Experience writing clinical protocols, Investigator Brochures, clinical study reports, eCTD clinical summaries, and integrated summaries. 5. Ability to present clinical data clearly; strong communication skills; proficiency in Microsoft Word. 6. Strong command of English language, grammar, style, and logical progression. 7. Ability to write concisely and persuasively, and to edit on all levels. 8. Experience with document templates, toolbars, and version control. 9. Demonstrated leadership, teamwork, communication, project management, and organizational skills; strong attention to detail.

Benefits

- Competitive salaries - Annual performance-based bonuses - Equity-based incentive program - Generous vacation - Paid wellness days - Support for learning and development