(Senior) Specialist Clinical Patient Supply Chain*
at immatics
72076 Tübingen, Baden-Württemberg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
OVERVIEW
We are currently seeking a (Senior) Specialist Clinical Patient Supply Chain* on a part-time basis to support our Global Patient Supply department. You will work in Tübingen, Munich or remote (from Germany) in an interdisciplinary environment with colleagues from Germany and the US. 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.
Responsibilities:
- Work cross-functionally between clinical operations, manufacturing, and quality to effectively manage patient products from starting material collection through drug product infusion
- Develop and improve SOPs, work instructions, and training materials which are used to ensure a seamless end-to-end patient journey
- Support clinical trial sites as primary point of contact for scheduling and general inquiries regarding patient journey activities
- Ensure chain of custody and chain of identity measures are maintained throughout all patient journey activities
- Support Contract Development and Manufacturing Organizations’ activities which include logistics support for all patient related material
- Manage auxiliary medicinal products as applicable for support of current clinical trials
- Support end-to-end supply chain operations including inventory through an IRT system
- Support planning and managing of clinical supplies for assigned clinical trial
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
72076 Tübingen, Germany