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Niche ADaM/CDISC skillset and seniority reduce competition, but metro role and hybrid posting increase candidate pool.
Clinical trial domain and CDISC/ADaM expertise strongly favor industry-specific experience, limiting cross-industry mobility.
Explicit 8+ years requirement plus mandatory SAS, ADaM and CDISC expertise makes filters strict.
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Develop custom SAS programs for ADaM datasets, TLFs, and clinical trial data outputs per statistical analysis plans and industry standards.
Lead and review programming deliverables ensuring quality, on-time delivery, and regulatory compliance including CDISC standards (SDTM, ADaM, DEFINE.XML).
Mentor and manage programming personnel, guide project planning, risk mitigation, and represent statistical programming in sponsor meetings.
8+ years of experience in Clinical SAS programming including Base SAS, Advanced SAS, SAS/Macros.
Strong experience in ADaM dataset and TLF programming and ADaM specifications.
Experience in client handling and leading clinical study programming teams.
Good knowledge of CDISC standards and regulatory submission requirements.
Experienced leader capable of managing multiple concurrent clinical trial programming projects and delivering complex programming solutions on time.
Subject matter expert in CDISC standards compliance and clinical trial data programming with ability to train and mentor others.
Skilled communicator comfortable interacting with sponsors and contributing in cross-functional team meetings including kickoff and bid defense.