Principal Statistical Programming Consultant (EU)
Core
Lead statistical programming for clinical trials, delivering high-quality outputs for early-phase studies, publications, and regulatory submissions.
Role type
Principal Statistical Programming Consultant (Clinical Trials)
Builds
SAS analysis datasets, tables, listings, and figures (TLFs) for Clinical Study Reports, safety reports, and efficacy reports
Domain
Clinical Research / Biostatistics / Oncology
Required skills
SAS programming, CDISC standards (SDTM, ADaM), data migration and transformation, TLF generation, regulatory compliance (FDA, EMA), oncology therapeutic area expertise
Preferred skills
Team leadership, mentoring programmers, global client environment experience, recruitment/interview process contribution
Technologies
SAS, CDISC (SDTM, ADaM)
Responsibilities
Develop and validate SAS analysis datasets, tables, listings, and figures; Lead at least one study team; Manage and mentor a small team of 2–4 programmers; Perform data validation and transformation according to client requirements; Collaborate with clients and global teams to resolve data issues and specification clarifications
Seniority
Principal, hands-on IC with leadership responsibilities
