Job Title: Trial Master File (TMF) Team Intern ">"> We are seeking a highly motivated and detail-oriented intern to join our Trial Master File (TMF) Team. As a TMF Intern, you will play a critical role in ensuring the organization, accessibility, and compliance of essential clinical trial documents. ">"> The ideal candidate will have a strong understanding of the drug development process and regulatory compliance standards. You will work closely with cross-functional teams to classify and organize documents within the TMF system, ensuring that they meet audit-ready and regulatory standards. ">"> You will also be responsible for analyzing deliverable metrics to identify trends and areas for improvement in document management. Additionally, you will contribute to reporting and tracking of TMF deliverables to support project timelines and quality standards. ">"> This is an excellent opportunity to gain hands-on experience in document management and contribute to the success of clinical trials. If you are a proactive, enthusiastic, and eager-to-learn individual with strong attention to detail and analytical skills, we encourage you to apply. ">"> About Us: ">"> Fortea is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. ">"> We are committed to transforming drug and device development for partners and patients across the globe. Our team is dedicated to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. ">"> Key Responsibilities: ">">