Teamlead Programming and Visualization

The Position

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

Requirements

• 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

Ready to contact us?

If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: +49 (0) 6132 77-3330 or via mail: hr.de@boehringer-ingelheim.com

Recruitment process:

Step 1: Online application - The job posting is presumably online until March 17th.
Step 2: Virtual meeting mid of March/End of March
Step 3: On-site interviews beginning of April

Discover our Biberach site: xplorebiberach.com