Manager, Data Programming, Analytics, and Reporting (m/f/d) in München

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines.

With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Location

• Primany location: France
• Second location: Germany
• Roles and Responsibilities
• Lead delivery of high-quality, timely clinical data management programming outputs across assigned studies, including reports, listings, visualizations, and data validation deliverables.
• Serve as a subject matter expert in clinical programming, reporting, data listings, database extracts, and visualization tools.
• Develop, review, test, and maintain programming specifications, standard/custom programs, templates, and validation scripts in compliance with programming and regulatory standards.
• Partner with study data managers and cross-functional stakeholders to define requirements, confirm specifications, and support ad hoc reporting and external data needs.
• Oversee complex study deliverables such as edit checks, patient profiles, subject narratives, discrepancy reports, dose modification reports, and exception listings.
• Identify, manage, and resolve risks or issues affecting data quality, integrity, timelines, and regulatory submission readiness.
• Support critical study milestones, including interim analyses, database lock activities, medical coding support, and inspection/audit readiness.
• Mentor and train team members, provide technical guidance, and support use of data visualization tools.
• Drive continuous improvement by contributing to SOPs, policies, standards, reusability, process efficiency, and quality metrics.
• Promote collaboration, Daiichi Sankyo values, and strong working relationships with internal teams, external partners, and vendors.

Education & Experience

• Bachelor’s degree or higher in life sciences or a related field.
• 5 to 8 years of global clinical trial experience in pharmaceutical, device, or CRO environments.
• Strong expertise in clinical programming methods, techniques, and data validation/reporting processes.
• Hands-on experience with reporting and visualization tools such as SAS, Spotfire, Tableau, and JReview.
• Knowledge of clinical data standards, including CDISC, CDASH, and SDTM/ADa M.
• Familiarity with clinical systems and technologies such as EDC, CTMS, IRT, Veeva Vault, RAVE, and In Form.
• Strong skills in project management, validation, QC/testing, documentation, and archival of clinical data programming deliverables.
• Demonstrated ability to work independently, manage multiple priorities, solve complex problems, and collaborate across functions, cultures, and experience levels.

Why work with us?

Working at Daiichi Sankyo is more than just a job – it is your chance to make a difference and change patients’ lives for the better.

We can only achieve this ambitious goal together.

That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity.

Here, you will have the opportunity to grow, think boldly, and contribute your ideas.

If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application.