Freelance Senior Statistical Programmer (Biotech) Start: ASAP * Location: Bavaria * Industry: Biotech / Pharma For our client we are looking for an experienced Senior Statistical Programmer to support our Biostatistics & Data Management team on a project basis. Required Qualifications Bachelor's degree in a relevant field (advanced degree preferred) 10 years of statistical programming experience in CRO/biotech/pharma Strong expertise in SAS, SDTM, ADaM, and CDISC standards Deep understanding of clinical trial reporting and regulatory submissions Hands-on experience with TFLs, define.xml, reviewer's guides, annotated CRFs Strong analytical & communication skills Proactive, entrepreneurial mindset; comfortable in fast-paced environments Key Responsibilities Oversee and manage statistical programming deliverables (internal & CRO) Perform hands-on programming and validation (SDTM, ADaM, TFLs) Lead statistical programming activities for regulatory submissions Develop timelines and collaborate closely with study statisticians Review SAPs, CRFs, DTA/DTS, and data management plans Own SDTM/ADaM specifications for assigned studies Mentor junior team members and support process improvement Contribute to building a common clinical database If you are a senior-level statistical programmer and ready to take on a high‑impact project, we'd love to hear from you. Please apply and share your profile and availability. SThree_Germany is acting as an Employment Business in relation to this vacancy.