Medical Writer

About the job

Telix Pharmaceuticals is a dynamic fastgrowing radiopharmaceutical company with offices in Australia (HQ) Belgium Japan Switzerland and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international rollout of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinicalstage products that address significant unmet need in oncology and rare diseases.

We are seeking an engaging and experienced Medical Writer or Senior Medical Writer. This position offers a unique opportunity to contribute to the achievement of Telixs strategic goals by leading and driving the writing process to accelerate clinical development of diagnostic and therapeutic assets in areas of high unmet medical need.

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 crossfunctional colleagues.

The Medical Writer will identify engage and project manage the work of contract medical writers as required.

What Youll Do

• Lead the compilation writing and editing of highquality clinical study synopses minutes of advisory boards and study steering committees and clinical sections of regulatory documents
• Interpret data search and analyze published literature define problems establish facts draw valid scientific conclusions propose solutions or corrective actions and compose text accordingly.
• Work with colleagues physicians clinical scientists and statisticians in a professional and organized manner to complete projects in a timely manner.
• Collaborate with project teams to respond to heath authority questions and requests.
• Develop and update pertinent SOPs processes templates style guides and manuals as needed.
• Maintain knowledge to enable ongoing execution of function as medical writing expert.

About You

• Bachelor of Science a science or related field required; masters or PhD preferred.
• 8 years of experience in pharmaceutical industry with 5 years of experience in regulatory writing required for Medical Writer; 8 years experience in regulatory writing required for Senior Medical Writer
• Strong understanding of drug development clinical study design regulations (CFR FDA EMA and ICH guidelines) and scientific principles. Understanding medical terminology and statistical methodology is a must.
• Experience writing clinical study synopses minutes and clinical sections of regulatory documents.
• Experience and proficiency with document templates document toolbars and proper version control.
• Strong project management skills. Organized and selfmotivated. Strong attention to detail.

Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

/jobs/view/d0f91d58779fa110d0d35b051eaf5ac4

Remote Work :

No