Full-Time Medical Writer
Telixus is hiring a remote Full-Time Medical Writer. The career level for this job opening is Experienced and is accepting USA based applicants remotely. Read complete job description before applying.
Telixus
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Job Details
Telix Pharmaceuticals is a fast-growing radiopharmaceutical company.
The Medical Writer will lead and drive the writing process, supporting clinical drug development. Responsibilities include planning and preparing clinical and regulatory documents for all phases.
Key Responsibilities:
- Compile, write, and edit high-quality regulatory documents (e.g., CSRs, IBs, safety narratives).
- Interpret data and literature, draw conclusions, propose solutions.
- Collaborate with colleagues, physicians, scientists, and statisticians.
- Respond to health authority questions and requests.
- Develop and update SOPs, templates, and style guides.
- Maintain knowledge of clinical development pipeline.
Qualifications:
- Bachelor's degree in science or related field; advanced degree preferred.
- 5+ years of regulatory medical writing experience.
- Strong understanding of drug development, regulations, and scientific principles.
- Experience with clinical protocols, Investigator Brochures, clinical study reports, eCTDs, and safety/efficacy summaries.
- Strong communication, interpersonal, and project management skills.
- Proficiency in Microsoft Word.
Key Capabilities:
- Inclusive mindset
- Creativity and innovation
- Commitment to excellence
- Results-oriented
- Ethical behavior
- Adaptability
- Strong communication skills
- Collaboration
- Resilience
- Continuous learning
Benefits:
- Competitive salary with bonuses and equity