Medical Writer
December 13
Description
• Contribute to Telix's goals by leading the writing process • Plan and prepare clinical and regulatory documents for drug development • Organize, analyze, and interpret scientific and statistical data for various documents • Collaborate with colleagues and project teams to complete writing tasks • Maintain knowledge of medical writing and Telix's development pipeline
Requirements
• Bachelor of Science in a science or related field required; Advance degree preferred • 5+ years of experience in regulatory medical writing required • Strong understanding of drug development, clinical study design, regulations, and scientific principles • Experience writing clinical protocols, Investigator Brochures, clinical study reports, and eCTD summaries • Ability to accurately present clinical data; strong communication skills and proficiency in Microsoft Word • Strong command of English language and writing abilities • Experience with document templates and version control • Demonstrated leadership capability and project management skills
Benefits
• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development
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🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🦅 H1B Visa Sponsor
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