Fortrea offers innovative solutions for delivering life-changing treatments to patients more quickly. As a global contract research organization (CRO) with extensive experience in clinical development, we provide pharmaceutical, biotechnology, and medical device customers with comprehensive clinical development, patient access, and technology services across diverse therapeutic areas.
We seek experienced professionals who share our commitment to scientific excellence. This role demands collaboration, teamwork, and exceptional communication skills. The ideal candidate will have advanced degrees, at least 6 years of eCTD submission writing experience, including 3 years as a medical writing project lead.
The selected individual will play a key role in leading the authoring and development of high-complexity clinical regulatory documents for our partners.
Our team is dedicated to revolutionizing the development process, ensuring swift delivery of life-changing ideas and therapies to patients in need.