Scientist Translational Research and Biomarkers* at immatics
72076 Tübingen, Baden-Württemberg, Germany -
Full Time


Start Date

Immediate

Expiry Date

21 Mar, 25

Salary

0.0

Posted On

17 Nov, 24

Experience

0 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

OVERVIEW

We are currently seeking a Scientist Translational Research and Biomarkers* to support our team in the development of innovative immunotherapeutic products. You will work in a full-time and permanent position on-site Tübingen (Germany) in an interdisciplinary environment with colleagues from all research as well as business development and intellectual property departments.

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
  • Planning, supervision, documentation and reporting of clinical Immunomonitoring data using a wide range of standardized cellular, non-cellular and molecular techniques
  • Method development in the context of translational research and clinical Immunomonitoring
  • Professional supervision of lab personnel being responsible for assay conduction
  • Development and management of assigned projects including communication with external vendors and the internal project team
  • Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.)
  • Support of Quality Management including writing and reviewing of Standard Operating Procedures (SOPs)
  • Contribution to preparing regulatory documents
  • Optional: Establishment of GCLP-relevant processes
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