Lead clinical trial SAS programming (Phase II-IV). Create & validate CDISC SDTM, ADaM, TLFs, & regulatory deliverables (Define.xml, eCRT). Manage project timelines, mentor junior staff, & support multi-disciplinary clinical study teams.
Required Candidate profile
5–9 yrs clinical/CRO experience with 5+ yrs in SAS. Expertise in end-to-end SDTMs/ADaMs, TLFs, & 2+ therapeutic areas (including oncology). Robust background in statistics or CS.