About Fortrea
Fortrea, a leading global Contract Research Organization (CRO), is dedicated to scientific excellence and boasts extensive experience in clinical development. We offer a broad range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With a team of over 19,000 professionals operating in over 90 countries, Fortrea is at the forefront of transforming drug and device development worldwide.
Position Overview
We are looking for a motivated and detail-oriented professional to join our team, where you will play a key role in supporting and executing high-quality clinical studies. You will ensure timely and accurate monitoring and reporting, support the implementation of new monitoring tools, and contribute to process improvements.
Key Responsibilities
Why Join Us?
At Fortrea, we are committed to overcoming barriers in clinical trials and revolutionizing the development process to deliver life-changing therapies to patients. Join our dynamic team and experience a collaborative environment where personal growth is fostered, enabling you to make a significant global impact.
Equal Opportunity Employer
Fortrea is proud to be an Equal Opportunity Employer. We value diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind. Employment decisions are based on business needs and individual qualifications, and we welcome applications from all individuals regardless of race, religion, color, national origin, gender (including pregnancy and medical conditions), family or parental status, marital status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
For more information on how we handle your personal data, please refer to our Privacy Statement.
Learn More
To learn more about Fortrea and our innovative work in clinical trials, visit www.fortrea.com.
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