As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Fortrea 2025 University Internship Program Trial Master File (TMF) Team Location: Maidenhead (office-based) Full-time, 12-month Start Date: July 2025
What if you could apply your scientific knowledge and organizational skills to advancing clinical research and ensuring compliance with regulatory standards?
About the TMF Team
The Trial Master File (TMF) Team is integral to the success of clinical research by ensuring the organization, accessibility and compliance of essential clinical trial documents. As a TMF Intern, you’ll work closely with TMF operations and cross-functional teams to uphold the quality, accuracy, and audit readiness of trial documentation. This role provides an excellent opportunity to gain hands-on experience in document management and contribute to the success of clinical trials.
Internship Assignment Summary
Learn the Basics:
Attend training sessions to understand the drug development process and how clinical trial documentation supports regulatory compliance. Document Management:
Assist in document classification and organization within the TMF system to ensure documents are audit-ready and meet regulatory standards. Metrics Analysis:
Analyze deliverable metrics to identify trends and areas for improvement in document management. Cross-functional Collaboration:
Work with TMF operations and other teams to address documentation needs and challenges. Reporting Assistance:
Contribute to reporting and tracking of TMF deliverables to support project timelines and quality standards. Shadow and Support:
Engage with senior team members to understand the strategy behind TMF operations, gaining knowledge and skills in this critical area of clinical research.
Education/Qualifications/Skills
Working toward a bachelor’s or master’s degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field. Strong attention to detail and analytical skills, with familiarity in MS Office, especially Excel. Proactive, enthusiastic, and eager to learn in a structured environment. Excellent communication and organizational skills to manage accuracy-focused tasks and collaborate effectively with cross-functional teams. Experience delivering projects in an academic or professional setting is a plus.
Join us to create lasting value for our stakeholders and make a meaningful impact on global health!
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
Equal Opportunity Employer
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact:
taaccommodationsrequest@fortrea.com . Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
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Fortrea 2025 University Internship Program Trial Master File (TMF) Team Location: Maidenhead (office-based) Full-time, 12-month Start Date: July 2025
What if you could apply your scientific knowledge and organizational skills to advancing clinical research and ensuring compliance with regulatory standards?
About the TMF Team
The Trial Master File (TMF) Team is integral to the success of clinical research by ensuring the organization, accessibility and compliance of essential clinical trial documents. As a TMF Intern, you’ll work closely with TMF operations and cross-functional teams to uphold the quality, accuracy, and audit readiness of trial documentation. This role provides an excellent opportunity to gain hands-on experience in document management and contribute to the success of clinical trials.
Internship Assignment Summary
Learn the Basics:
Attend training sessions to understand the drug development process and how clinical trial documentation supports regulatory compliance. Document Management:
Assist in document classification and organization within the TMF system to ensure documents are audit-ready and meet regulatory standards. Metrics Analysis:
Analyze deliverable metrics to identify trends and areas for improvement in document management. Cross-functional Collaboration:
Work with TMF operations and other teams to address documentation needs and challenges. Reporting Assistance:
Contribute to reporting and tracking of TMF deliverables to support project timelines and quality standards. Shadow and Support:
Engage with senior team members to understand the strategy behind TMF operations, gaining knowledge and skills in this critical area of clinical research.
Education/Qualifications/Skills
Working toward a bachelor’s or master’s degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field. Strong attention to detail and analytical skills, with familiarity in MS Office, especially Excel. Proactive, enthusiastic, and eager to learn in a structured environment. Excellent communication and organizational skills to manage accuracy-focused tasks and collaborate effectively with cross-functional teams. Experience delivering projects in an academic or professional setting is a plus.
Join us to create lasting value for our stakeholders and make a meaningful impact on global health!
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
Equal Opportunity Employer
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact:
taaccommodationsrequest@fortrea.com . Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
#J-18808-Ljbffr
