Senior Medical Writer

Overview

Sponsor-dedicated. Full time. Remote in the UK, Greece, Spain or Portugal. We are on a mission to deliver solutions that bring life-changing treatments to patients faster. 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. This is why we need you. Join Fortrea. Your job matters.

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. We´ll trust you to spearhead the entire process, from initial planning and coordination through all stages of development, culminating in the final delivery to the sponsor. From the variety of documents you will work on (Inves...