Entry dated April 14, 2026

RHEACELL offers a talented scientific statistician* a unique opportunity to take on a central role in methodological development and capacity building, strengthen the biostatistics department and support interdisciplinary teams. The position is based in Heidelberg.

The biostatistics department covers the areas of biomedical informatics, health biostatistics, statistical innovation and scientific computing. It works closely with medical and clinical teams to improve decision-making processes in drug development through applied data science.

In the role of biostatistician*, you identify and drive the development and application of analytical methods, skills, tools, processes and best practices. The aim is to provide robust, regulatory-compliant and scientifically sound findings to support approval processes and optimize production processes.

As a biostatistician, you play an essential role in a multidisciplinary biostatistics department (including statisticians*, data managers*, programmers*) and ensure seamless integration of external service providers and Contract Research Organizations (CROs).

Professional Focus

• Analysis and interpretation of clinical study data (especially phase III data), as well as data from manufacturing processes (batch records, product quality reviews)
• Conducting statistical analyses (such as primary and secondary endpoints, survival analyses, mixed models/repeated measures)
• Preparation and review of statistical analysis plans (SAPs), randomization plans and sample size calculations (power analyses)
• Support in the preparation of Clinical Investigation Reports (CIRs) and study protocols
• Consideration of EMA and FDA guidelines and support in the preparation of regulatory dossiers
• Ensuring regulatory compliance (ICH-GCP) and internal standards
• Close collaboration with Clinical Science, Clinical Operations and Regulatory Affairs

Your Building Blocks for Joint Success

• Completed studies in statistics/biostatistics or mathematical statistics, ideally with pharmaceutical experience
• Experience with innovative statistical solutions in the clinical development environment, particularly in designing, analyzing, and interpreting clinical studies and clinical study programs
• Professional knowledge and experience in R and SAS (programming languages/environments) for conducting statistical analyses
• Broad awareness of statistical issues in the context of evolving scientific and regulatory requirements
• A high level of competence in global and interdisciplinary collaboration
• Ideally, prior experience in immunology and inflammation, as well as rare diseases
• Excellent oral and written communication and presentation skills in English (C2); German is a clear advantage
• Strong initiative and a solution-oriented approach
• Team spirit and enjoyment in collaborating with diverse departments

What We Offer

• Full-time permanent position with attractive compensation
• A motivated, supportive, and collaborative team
• Opportunity to work with leading experts in clinical development, regenerative medicine, and ATMPs
• Collaborative and international working environment with strong scientific exchange
• Diverse training and professional development opportunities
• Flexible, individual mobility budget as well as free parking
• Complimentary beverages and fresh fruit for the workday
• Extensive corporate benefits
• Company pension scheme

Does this sound like a work culture that suits you?

Then we look forward to getting to know you! Please send your complete application documents (cover letter, CV, certificates) stating your salary expectations and earliest possible starting date.