Specialist / Coordinator Biological Sample Management*
at Immatics Biotechnologies GmbH
72076 Tübingen, Baden-Württemberg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 05 Jul, 2024 | Not Specified | 05 Apr, 2024 | N/A | Good communication skills | No | No |
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Description:
OVERVIEW
We are currently seeking a Specialist / Coordinator Biological Sample Management* to strengthen our Target Bioanalytics department. You will work in Tübingen (Germany) in an interdisciplinary environment with colleagues from Germany and the US (Houston, TX). Within the Target Bioanalytics department, the sample management team is responsible for maintaining the oversight of commercially procured human tissue samples as well as clinical trial patient samples across preclinical research and clinical departments. You can expect a variety of tasks in a dynamic team with great enthusiasm for our work and community spirit at Immatics. You will contribute to the team’s success through your pro-active thinking and attitude, your organizational skills as well as your commitment.
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:
- Sample logistics: Coordination of sample receipt, packaging and shipment to and from clinical sites, external partners and different departments within Immatics
- Management of sample documentation trackers and thereby keeping the overview of expected, received and analyzed samples
- Paper-based GCP-compliant documentation and extraction of relevant information from patient pathology reports
- Supporting activities required in a routine laboratory, especially for the sample processing, storage and archiving
- Preparation of FFPE sections for patient enrollment in clinical trials
- Opportunity to expand experimental skills into additional method area
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
72076 Tübingen, Germany