We're seeking a highly motivated Pharmaceutical Trial Management Intern to join our team and contribute to the success of clinical trials. As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with clinical development, patient access, and technology solutions across 20+ therapeutic areas.
The Trial Master File (TMF) Team plays a critical role in 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.
Your Key Responsibilities Will Include:
* Learning and Development: Attend training sessions to understand the drug development process and how clinical trial documentation supports regulatory compliance.
* Document Classification and Organization: Assist in document classification and organization within the TMF system to ensure documents are audit-ready and meet regulatory standards.
* Metrics Analysis and Reporting: Analyze deliverable metrics to identify trends and areas for improvement in document management, and contribute to reporting and tracking of TMF deliverables.
* Cross-functional Collaboration: Work with TMF operations and other teams to address documentation needs and challenges.
You'll Be Well-Suited for This Role If You Have:
* 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.