OVERVIEW

We are currently seeking full-time a Senior Clinical Data Manager* to support our global team. You will work in Tübingen, Munich or remote (Germany) in an interdisciplinary environment with colleagues from Tübingen, Munich and Houston (USA). This permanent position is responsible for driving and managing data management activities for clinical trials.

ABOUT US

Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. Operating from Tuebingen, Munich and Houston, we are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer. For more detailed information, visit www.immatics.com.

• Act as Project Data Manager: Plan, set-up, conduct and close-out of clinical trial data management activities within timelines and budget
• Perform and/or oversee Data Management hands-on tasks as Trial Lead Data Manager: Preparing, reviewing releveant documents (e.g. DMP, Coding Plan, Reconciliation Plan, etc.)
• Perform and/or oversee and manage the development, implementation and change management of clinical data management systems (e.g. eCRF, IRT, ECS, UAT Plan, UAT, Central Imaging, Central Laboratories, etc.)
• Deliver high quality data by meeting industrial requirement and standard, timelines and milestones
• Ensure the ongoing TMF filing to be inspection ready
• Review and input to clinical trial documents
• Oversee and manage centralized monitoring
• Participate in the defninition and implementation of eCRF/IRT standards
• Develop and maintain SOPs, guidance documents & training material for clinical data managemen