Internship in Clinical Project Management / Clinical Monitoring (m|f|d)

As an intern in Clinical Project Management / Clinical Monitoring, you will gain practical insights into the operational side of clinical studies and support our team in a variety of organizational and documentation‑related tasks. Your responsibilities include:

• Supporting Trial Master File (TMF) activities
  Helping with TMF planning, document handling, and simple reconciliation tasks to ensure study documentation is complete
• Preparing EndNote libraries
  Assisting with organizing and maintaining reference libraries for clinical documents
• Supporting the creation of functional plans
  Helping draft and structure operational plans used across clinical projects
• Assisting with TFL reviews
  Supporting the team in reviewing tables, figures, and listings to ensure accuracy and consistency
• Helping maintain trackers
  Working with CPMs/CTMs and other functions (e.g., labs) to set up or update study‑related tracking tools
• Supporting contract and vendor management tasks
  Assisting with general oversight activities and coordination—not limited to study‑specific tasks
• Preparing Master ISF and Site ISF documents
  Helping organize essential study materials for investigational sites
• Providing support to CRAs
  Sharing EDC listings and query reports to help monitor study progress