Immatics

(Senior) Manager Biostatistics*

Tübingen, BW, DE

about 2 months ago
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Summary

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. We are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer.





OVERVI


EW
We are currently seeking a full-time (Senior) Manager Biostatistics* to join our Biostatistics Team in the Translational Science Department in Tübingen, Germany. In this role, you will work in an interdisciplinary environment, collaborating closely with clinical and non-clinical departments across our global organization. Your contribution will be essential in advancing our mission to develop innovative cancer immunotherapies that improve clinical outcomes for patients. Tübingen is a vibrant university city near Stuttgart in southern Germany. This is a permanent positi



on.

YOUR MI


SSION
Your main responsibilities will include but are not limited to the following

  • tasks:Leading biostatistical activities for one or more clinical trials, ensuring the planning, setup, execution and quality control of statistical outputs (tables, figures and listings) based on clinical trial data. You will generate respective texts and discuss results within a cross-functional team to support the development of our drug candidates. Specific tasks include: Reporting and analyzing safety and efficacy data; Contributing to the drafting of clinical and regulatory study documents; Answering translational/exploratory questions; Supporting the publication of clinical tria
  • l dataProviding statistical expertise throughout the entire lifecycle of our clinical programs, including clinical study protocol design, statistical analysis plan (SAP) development, preparation of interim data readouts, and completion of clinical study re
  • ports.Ensuring accurate and complete data collection in the Electronic Data Capture (EDC) systems, working closely with the data management
  • team.Supervising external vendors to ensure that biostatistical outputs (SDTM, ADaM, TFLs) meet expected standards and align with the analyses described in the protocol an
  • d SAP.Contributing to continuous improvement of data analysis workflows, as well as implementing and executing quality measures to ensure data integrity, in close collaboration with other clinical



teams.

YOUR


  • PROFILE
    Master’s degree or PhD in statistics, data science, life science, or in a related field, ideally with a focus on clinical biostatistics and statistical pro
  • gramming.At least 1 year of Industry experience in analysis and reporting of clinical tr
  • ial data.Strong attention to detail with strong affinity to answer scientific q
  • uestions.Hands-on experience with programming in SAS, R and good programming practices is an a
  • dvantage.Familiarity with applicable clinical research regulatory requirements, such as GCP and ICH guidelines, is p
  • referred.Ability to work independently, apply analytical reasoning, and communicate effectively in
  • English.Basic knowledge of immunology, oncology and/or cell and gene therapy i



s a plu


s.

WHY US?
We are a committed and inspired team and cherish the collegial, highly motivated and family-friendly atmosphere within Immatics. Our culture allows for a high level of originality, independent thinking and initiative. We believe in supporting our employees’ professional and social skills: We enable them to join conferences and trainings as well as to enjoy our Immatics benefits – e.g. job bike, job ticket, Health Programs, childcare benefits, relocation allowance, Company summer and wi



nter e


vents.

NOTICE
*We value diversity and inclusion. Immatics N.V. and all Immatics subsidiaries are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics pr


otected by law.

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