Job Description

Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T-cell product, is currently undergoing pivotal clinical trials on a global scale.

Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages.

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

Qualifications

• You are an enrolled student in life sciences, health sciences, or a data‑related field.
• Interest in clinical research and working with data
• Careful, detail‑oriented working style
• Willingness to learn new software tools
• Good English and German skills
• Reliable, proactive mindset
• Your workplace will be Bergisch Gladbach.

Additional Information

The internship can be voluntary or mandatory - as you require.

What we offer

• A modern workplace in Bergisch Gladbach with opportunity for some mobile work. Exciting opportunities in the development of technologies with a secure future.
• Cross-border intercultural cooperation and short communication channels
• A collegial corporate culture and flexible working hours enable time management on your own terms
• Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University
• Diverse corporate benefits with regard to employee health, sport, and staff events

We look forward to your application

If you want to work in an open, creative and supportive team, this is the place for you. We look forward to receiving your application along with your salary expectations and availability.