OVERVIEW

We are currently seeking a full-time (Senior) Clinical Statistical Programmer – SAS* to join our Biostatistics Team in the Translational Science Department located in Tübingen, Germany. The position is available immediately and can be based in Tübingen, in Munich or remote (Germany). In this role, you will work in an interdisciplinary environment, collaborating closely with clinical departments across our global organization and will contribute to our mission of delivering novel PRAME immunotherapies to patients with cancer. This is a permanent position.

YOUR MISSION

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

Data Preparation, Standardization, and Statistical Output Generation

• Collaborate with biostatisticians to develop, validate, and review Table, Figures and Listings (TFLs) for our clinical studies.

• Work closely with biostatisticians and data managers to clarify data specifications and address data quality issues.

• Ensure together with biostatisticians the timely and accurate delivery of statistical outputs in alignment with protocol requirements and project timelines.

• Support the programming implementation of Statistical Analysis Plans, including mock TFLs and derived datasets.

• Support the development, review and validation of CDISC compliant SDTM and ADaM datasets.

Quality, Compliance, and Regulatory Submission

• Participate in documentation, TMF filing, and compliance activities in accordance with Good Clinical Practice (GCP), ICH guidelines, and internal SOPs.

• Contribute to the preparation and quality control of statistical outputs, regulatory submission packages, and Clinical Study Reports, ensuring full traceability, consistency, and compliance with applicable standards.

Process Optimization and Quality Assurance

• Contribute to the continuous improvement of data analysis workflows by identifying opportunities for greater efficiency and standardization.

• Develop and apply robust quality control measures to ensure the integrity, reproducibility, and regulatory compliance of all statistical programming outputs, in close collaboration with cross-functional clinical teams.

YOUR PROFILE

• Bachelor’s or Master’s degree in statistics, data science, life sciences, or a related field, ideally with a focus on statistical programming.

• Strong proficiency in SAS in a clinical research setting is required, with experience in R considered a plus. A solid understanding of best programming practices is essential.

• Minimum 3-5 years of industry experience as a statistical programmer.

• Familiarity with applicable clinical research regulations such as GCP and ICH guidelines is preferred.

• Strong attention to detail and a highly structured, methodical working style.

• Ability to work independently, apply analytical thinking, and communicate clearly and effectively in English, German language skills are a plus.

• Basic knowledge of immunology, oncology, and/ or cell and gene therapy is a plus.

WHY US?

We are the global leader in precision targeting of PRAME. Driven by our mission to make an impact on the lives of patients with cancer, 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 winter events.

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 protected by law.