(Associate) Manager for Sample Management*

at  immatics

OVERVIEW

We are currently seeking a(n) (Associate) Manager for Sample Management* to support our Translational Research and Biomarkers team in the development of innovative immunotherapeutic products. You will work in Tuebingen (Germany) in an interdisciplinary environment with colleagues from research and clinical development departments. Your analytical reasoning and action-oriented style as well as your organization and communication skills will contribute to the team’s success.

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.

• You are responsible for clinical trial sample management in a GCP environment.
• You are the main point of contact for Immatics stakeholders and logistics partners, promoting synergies and transparency.
• You liaise with external partners and organize remote or on-site trainings, while ensuring contractual obligations are met.
• You coordinate
• Sample shipment, handling and receipt from clinical sites, working with external partners and different departments within Immatics.
• PBMC sample processing with clinical sites.
• Sample processing with external partners (e.g., PBMC isolation).
• Distribution of material to external partners.
• You are responsible for streamlining processes across all different sample types.
• You manage/ own central documentation tools/ central trackers and thereby keep the overview of expected received and analyzed samples.
• You review all sample-associated sections of clinical trial documents (e.g., laboratory manual, SOPs)