Senior Biostatistician (m|f|d)

Join us in shaping the future of biomedicine and make cancer history. For more than 30 years, we have been developing cutting-edge science and technology to empower biomedical research and personalized medicine. We combine excellence from more than 60 disciplines in natural sciences, engineering, and informatics to make a significant contribution to biomedical sciences. We encourage a creative working environment driven by pioneering spirit – to seek new horizons – boldly envisioning the future and turning it into reality. Today, more than 4,400 experts from over 50 countries contribute to our sustainable success.

As part of the Cell Therapy Analytics Development Team in the R&D department you will support an interdisciplinary group of colleagues who are happy to join forces with you to develop the next generation of anti-cancer therapies by implementation of statistical models and data analysis.

• You will perform statistical analyses, validate analytical results and provide statistical models for assay set.
• You will provide statistical input for the development of analytical methods and their integration into preclinical and clinical projects in our CAR T-cell pipeline, including regulatory submission documents.-up and verification for quality control of cellular drugs.
• You develop, establish and improve statistical processes, analysis plans, data management and standards within the R&D department.
• You will work both independently and in close collaboration with colleagues from other R&D teams and other departments, e.g. pharmaceutical development and quality control groups.

• You have a PhD in statistics, biostatistics or bioinformatics and have several years of experience in the pharmaceutical/biotechnology industry and/or CRO, preferably in the field of cell and gene therapy with experience in regulatory submissions.
• You bring excellent knowledge of statistical methods and data analysis with statistical software such as SAS, JMP, R and others and you are familiar with regulatory guidelines (ICH, FDA, EMA).
• You work proactively, goal-oriented and independently, but at the same time also interdisciplinary in a team and are able to handle multiple projects of varying complexity, balance priorities and meet tight deadlines.
• You are passionate about scientific work that has the potential to bring meaningful benefits to patients and contribute to the development of the next cancer therapeutics.
• You impress with excellent communication and presentation skills as well as a good command of written and spoken English.

If you have the skills and qualifications for this position, please use the link to send us your details (application letter, curriculum vitae, references and certificates).

Please give us some idea of when you can start and the kind of salary you are looking for.