Remote Jobs at Fortrea
Find your next remote opportunity · 8 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.
Regulatory Affairs Project Manager
Project Manager overseeing regulatory affairs in the pharmaceutical industry at Fortrea. Managing budgets and ensuring compliance with regulatory guidelines in a remote US position.
Delivery Director – Immunology, Respiratory
Director level position overseeing clinical delivery across a portfolio of studies in biopharmaceuticals. Engaging with leadership to improve operations and client relationships.
Senior Manager – Workday Integrations and Reporting
Workday Reporting & Integrations Lead responsible for integrations and reporting in Workday systems at Fortrea. Leading a team and collaborating with business stakeholders to ensure data insights and system connectivity.
Senior Manager, Workday Security
Workday Security Senior Manager overseeing Workday security architecture and compliance for Fortrea. Collaborating with HR, Finance, IT, and Compliance teams to safeguard sensitive data access.
IT Manager
IT Manager responsible for Medidata Rave support and enterprise data platform activities. Collaborating with internal teams for operational support and maintaining data integrity.
Principal Statistical Programmer – Sponsor Dedicated
Principal Statistical Programmer in sponsor-dedicated Flexible Solutions business unit for global pharmaceutical company. Overseeing programming activities in clinical trials with opportunities for career growth.
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.
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