Job Purpose
As a Medical Writer, you are an integral part of MoonLake’s Clinical Development team responsible for providing medical writing support to our clinical development programs including preparation, development, review, revision and finalization of clinical, medical and regulatory documents for submission to external stakeholders and communities.
Key responsibilities:
- Prepare, edit and review medical, regulatory and clinical documents to sup-port MoonLake’s development programmes including clinical study protocols, investigator brochures, non-clinical summaries, briefing documents, safety/efficacy summaries, clinical study reports and modules for a biologics license application.
- Drive and coordinate the development of cross-functional documents to en-sure completion to timelines.
- Support cross functional project teams by providing medical writing consul-tancy on various aspects and provide advice on Medical Writing issues and help to resolve problems.
- Research and develop clinical and medical materials, ensuring that outputs are appropriately referenced and accurate in content and editorial style.
- Work closely with subject matter experts to ensure their writing is of the highest standard of technical accuracy.
- Develop and support QC processes to ensure quality and accuracy within and between development documents.
- Assist in the development of templates for core documents that ensure the compliance and consistency.