Statistical Programmer 2
Core
Lead statistical programming for clinical trials, producing analysis plans, datasets, tables, listings, figures, and study reports while mentoring junior staff.
Role type
Senior Statistical Programmer (Team Lead)
Builds
Statistical analysis outputs (TLFs), Clinical Study Reports (CSRs), and analysis plans for clinical trials.
Domain
Clinical Research / Biostatistics
Required skills
SAS programming, CDISC/ADaM standards, Statistical Analysis Plan (SAP) authoring, Data Management, Clinical Study Report (CSR) drafting, Protocol statistical section review, Sample size calculation, Risk management, Budget and timeline planning, Mentorship
Preferred skills
StatXact, Randomization schedule review, Bid defense presentation, Cross-functional collaboration (via careerplan.io/jobs/R1563693-statistical-programmer-2-at-iqvia)
Technologies
SAS, StatXact, CDISC, ADaM
Responsibilities
Author or QC review SAPs and shells; Program datasets and TLFs per industry standards; Handle database lock/unblinding; Mentor junior staff; Manage study timelines and budgets; Review protocols and CSRs.
Seniority
Senior, hands-on IC with team lead responsibilities