Remote Regulatory Medical Writer II – Lead Complex Docs
Save this job and keep your search organized
Create a free account to save jobs, create alerts and return to this listing from your dashboard.
By continuing, you agree to our Terms & Privacy Policy.
Fortrea is seeking a Regulatory Medical Writer II to own high-complexity Phase II-IV clinical regulatory documents and drive them through planning, drafting, review and final delivery.
You will lead document planning, align stakeholders across Europe, the Americas and Asia-Pacific, and translate complex data into clear regulatory content. A Life Sciences degree is required; a PhD is preferred, with at least 3 years in regulatory medical writing and 1 year of project leadership.
-
Regulatory Medical Writer II
7 days ago
Durban, KwaZulu-Natal, South Africa Fortrea Full-timeFull time. Remote in the UK, South Africa, Greece, Portugal.Ready to take ownership of complex regulatory documents while working directly with some of the world's leading pharmaceutical companies?At Fortrea, we help bring life-changing treatments to patients faster.To do that, we need experienced Medical Writers who can lead document development, align...