About the Role
As a Medical Writer at Telix Pharmaceuticals, you will play a key role in supporting the company’s mission to deliver precision medicine for cancer and rare diseases. This position will lead the planning, preparation, and submission of clinical and regulatory documents across all stages of drug development.
You will collaborate with cross-functional teams including clinicians, statisticians, and project managers to produce high-quality, compliant documentation that supports global regulatory submissions and scientific communication.
Key Responsibilities
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Write, edit, and compile regulatory and clinical documents (CSRs, IBs, safety reports, eCTD summary documents, ISS/ISE, protocols).
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Interpret data, review scientific literature, and present findings clearly and accurately.
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Collaborate with clinical and regulatory teams to respond to health authority inquiries.
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Maintain knowledge of Telix’s development pipeline and current regulatory requirements (FDA, EMA, ICH).
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Contribute to SOPs, templates, and style guides for consistent documentation standards.
Qualifications
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Bachelor’s degree in science or related field (advanced degree preferred).
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5+ years of regulatory medical writing experience.
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Strong knowledge of clinical drug development, study design, FDA/EMA/ICH guidelines, and medical terminology.
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Proven experience drafting protocols, Investigator Brochures, study reports, and eCTD summaries.
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Excellent command of English grammar, style, and scientific communication.
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Proficiency in Microsoft Word, version control, and document management systems.
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Strong project management skills with ability to meet deadlines in a fast-paced environment.
Key Capabilities
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Inclusive mindset and ability to collaborate across diverse global teams.
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Strong communication and interpersonal skills.
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Resilience, adaptability, and problem-solving mindset.
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Commitment to ethical practices and continuous professional growth.
Why Join Telix?
Telix Pharmaceuticals is a fast-growing, global radiopharmaceutical company with a mission to improve the quality of life for people living with cancer and rare diseases. As part of our team, you’ll join a collaborative, inclusive, and purpose-driven culture dedicated to advancing precision medicine.