Safety Writer responsible for preparation and review of safety documents and effective communication with clients in pharmaceuticals industry.

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry.
We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need.
Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services.
Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.
Our talented and diverse team of approximately 19,000 people working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally.
Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
Browse and apply for open jobs at Fortrea.
Safety Writer responsible for preparation and review of safety documents and effective communication with clients in pharmaceuticals industry.
Clinical Research Associate at Fortrea monitoring global clinical trials. Collaborating with stakeholders to ensure patient safety and data integrity while adhering to regulatory guidelines.
Senior Manager of Global Sourcing at Fortrea leading strategic sourcing initiatives and managing Source to Contract process for Clinical Technologies. Collaborating with teams to drive value and align business objectives.
Clinical Research Associate overseeing clinical studies and ensuring compliance with Fortrea’s SOPs and regulatory standards. Involves site management, monitoring, and data integrity assurance.