Remote Jobs at Fortrea
Find your next remote opportunity · 7 Open Positions
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.
Senior Regulatory Medical Writer
Senior Regulatory Medical Writer leading development of clinical regulatory documents for a global pharmaceutical company. Collaborating with teams across Canada, Europe, the Americas, and Asia-Pacific.
Principal Regulatory Medical Writer
Principal Regulatory Medical Writer leading clinical regulatory document development for a top global pharmaceutical client. Committed to bringing life-changing treatments to patients faster.
Senior Marketing Manager
Marketing Senior Manager driving strategic marketing programs for Fortrea's healthcare solutions. Architecting integrated campaigns across paid and owned channels, ensuring analytics-driven performance improvement.
Workday PSA Architect
Workday PSA Architect managing Workday PSA solutions for financial operations. Collaborating with cross-functional teams to optimize processes and enhance user experience.
Assistant Clinical Quality Control Manager
Assistant Clinical Quality Control Manager for Fortrea's FSP team based in the US. Responsible for quality control data tracking and reporting while collaborating with various stakeholders.
Product Owner, CTMS, eTMF, SSU
Product Owner for Clinical Systems managing CTMS, eTMF, and SSU platforms in a clinical trial technology environment. Responsible for backlog management, stakeholder collaboration, and ensuring compliance.
Senior Statistical Programmer – Oncology
Senior Statistical Programmer developing SAS programs for global oncology clinical trials. Working remotely or from local offices to support life-changing oncology therapies.
No more jobs available.