Teamlead Programming and Visualization

Shape the future of clinical data - lead innovation in early-phase development As Team Lead Data Programming & Visualization , you will take on a pivotal leadership role at the heart of early-phase clinical development, with a strong focus on healthy volunteer studies. Guiding a growing team of experts, you will shape cutting-edge data analysis processes across first-in-human SRD/MRD studies, bioequivalence and bioavailability trials, drug-drug interaction studies, TQT designs, and more.

If you are ready to lead, innovate, and redefine what's possible in clinical data science - apply now and join us on this journey.

This position is hybrid with at least 1-2 days per week on site.

This position is part time eligible with 80 %.

Tasks & responsibilities

• You will lead a globally integrated team to ensure the delivery of high-quality datasets and analyses for studies in healthy volunteers covering first-in-man safety assessment as well as Clinical Pharmacology aspects across diverse therapeutic areas
• By fostering a collaborative and innovation-driven environment, you will strengthen global team leadership and enable technical excellence
• With your strategic perspective, you will shape the next generation of data analysis capabilities for early-phase clinical studies
• You will oversee descriptive analyses of subject disposition, efficacy, and safety, while also guiding inferential statistical evaluations across various study designs
• By aligning data analysis and reporting processes with cross-functional partners - such as ECG specialists and Clinical Pharmacology experts - you will help streamline key interfaces
• You will build strong connections across ExpMed, Clinical Pharmacology, IT, Regulatory Affairs, Quality Medicine, and BDS to support cohesive data workflows
• Through your contribution to agile and exploratory analysis approaches, you will enable rapid and data-driven decision-making within early development

Do you have experience in SAS?, Do you have a Master's degree?, * Master's degree or PhD in Biostatistics, Statistics, Data Science, or a related field, combined with longstanding and relevant experience in early-phase clinical data analysis

• Proven direct leadership experience in a global, dynamic environment
• Strong expertise in healthy volunteer studies and associated study types (e.g., SRD/MRD, bioequivalence, bioavailability, drug-drug interaction)
• Proficiency in statistical programming (e.g., SAS, R) and modern data visualization tools
• Solid understanding of regulatory standards (e.g., CDISC, FDA, EMA)
• Excellent communication and stakeholder-management skills, paired with intercultural competence and the ability to inspire teams
• Strategic, conceptual, and solution-oriented mindset, with enthusiasm for analytical and strategic work
• Fluency in English; German language skills are a plus or openness to learning German