As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Full time. Remote. UK, France, Spain or Portugal.

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 Principal 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.

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