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Ideally, you have experience in one of the above-mentioned areas of responsibility
Advanced verbal and written English language skills are required
Your independent, accurate working style and time management skills help you work with the highest degree of efficiency
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You value working in a structured and organized fashion and approach tasks with quick comprehension and foresight
You are a reliable and enthusiastic team player and are open to a high degree of flexibility in your tasks
Accurate documentation of workflows and results is of highest importance to you
You have successfully completed your apprenticeship or have an equivalent educational qualification in a life science/ medical field

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Industry experience in analysis and reporting of clinical trial data is a plus
Hands-on experience in programming in SAS, R, SQL and good programming practice are an advantage
Ideally, you gained knowledge of applicable clinical research regulatory requirements
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We expect a high degree of independent working, analytical reasoning, and good communication skills in English
Basic knowledge in immunology, oncology and/ or cell and gene therapy is a plus
You hold a 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 programming

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You hold a PhD or MSc degree in Bioinformatics or a related field
You have in-depth knowledge of statistics and data analysis
You are proficient in at least one scripting or programming language
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You maintain high code quality, including proactively writing tests and documentation
You have good communication skills in English and enjoy interdisciplinary collaboration
Knowledge of machine learning, databases, software development, peptidomics, or immunology is an advantage

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