Job Description
Sponsor‑dedicated. Full time. Remote in the UK, Spain, South Africa, Greece, Portugal or Hungary.
We are on a mission to deliver solutions that bring life‑changing treatments to patients faster.
But we can’t do it alone.
We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and development of high‑complexity clinical regulatory documents that are critical to the strategic projects of our partner. What You Will Do
Embedded in the team of one of the world’s leading pharma companies, you will be one of the primary Regulatory Medical Writers , project leading the development cycle for high‑complexity Phase II–IV clinical regulatory documents.
You will own the end‑to‑end medical writing process, from initial planning and cross‑functional coordination through drafting, review, and final delivery, ensuring alignment with project strategy, stakeholder expectations, and agreed timelines.
Your contribution will b...