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Delivering the Power of T Cells to Cancer Patients
Senior Clinical Statistical Programmer – SAS
Location
Germany
Posted
110 days ago
Salary
0
Seniority
Senior
Job Description
Senior Clinical Statistical Programmer – SAS
Immatics
• 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. • 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. • 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.
Job Requirements
- Bachelor’s or Master’s degree in statistics, data science, life sciences, or 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.
Benefits
- Health Programs
- Job bike
- Job ticket
- Childcare benefits
- Relocation allowance
- Company summer and winter events
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