Mathematician as Associate Director (m/f/d)

Das ist der Job

Train junior programmers and CRO staff on B

Darum lohnt es sich

Ensure accuracy of efficacy/safety outputs, perform quality control (QC), and resolve discrepancies in collaboration with Biostatistics and Data Management teams Serve as the primary programming point of contact for study teams Partner with Biostatistics to interpret analysis requirements, with Clinical Operations to address data issues, and with Regulatory Affairs to prepare submission-ready materials (e.g., ISS/ISE, CSR appendices) Manage relationships with outsourced programming partners (CROs), including scope negotiation, timeline oversight, and quality audits.

Associate Director Statistical Programming (Oncology) Mainz, Germany; London, United Kingdom; Munich, Germany; Paris, France; Randstad, Netherlands | full time | Job ID:8855 Lead the statistical programming deliverables (e.g., SDTM/ADaM datasets, tables, listings, figures) for assigned studies, ensuring alignment with protocols, statistical analysis plans (SAPs), and timelines.

Manage internal programmers or external vendors (CROs) to maintain quality, consistency, and compliance with CDISC standards and regulatory requirements Hands-on review, validation, and troubleshooting of SAS/R programs for data transformation, analysis, and reporting.

Anticipate resource needs and monitor resource allocation across studies to balance workload and ensure deliverables meet deadlines Develop and implement standardized macros, tools, or workflows to improve efficiency across studies.