Location: [Location]
Company: Fortrea
About Fortrea
Fortrea is a global leader in clinical research, dedicated to scientific rigor and decades of experience in clinical development. We offer pharmaceutical, biotechnology, and medical device customers a comprehensive range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With operations in over 90 countries and a team of 19,000+ professionals, Fortrea is at the forefront of transforming the drug and device development process, improving outcomes for both partners and patients worldwide.
Fortrea is looking for a Trial Master File (TMF) Document Specialist to join our team. In this role, you will be responsible for the management of eTMF (electronic Trial Master Files) and associated document classification tasks. This position will ensure all documents are processed, tracked, and maintained in compliance with regulatory requirements and company SOPs, contributing to the overall success of clinical trials.
Fortrea is committed to transforming the clinical development process and delivering life-changing therapies to patients. We encourage motivated and innovative problem-solvers to join our diverse and collaborative team. At Fortrea, you'll have the opportunity to grow both personally and professionally while contributing to groundbreaking clinical trials that make a real difference in patients' lives.
To learn more about Fortrea and explore career opportunities, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer. We strive to maintain an inclusive and diverse workforce and do not tolerate any form of discrimination. We make hiring decisions based on individual qualifications and the needs of our business, and we encourage all qualified individuals to apply, regardless of race, religion, color, gender identity, sexual orientation, or other protected characteristics.
For more information on how Fortrea collects and stores your personal data, please see our Privacy Statement.
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