Sr. Scientist Stat Programming, Late-Stage Development (Hybrid)

Responsibilities: Support statistical programming activities for late-stage drug/vaccine clinical development projects; may lead one or more projects. Develop and execute statistical analysis and reporting deliverables (safety/efficacy analysis datasets, tables, listings, figures) spanning trials through worldwide regulatory submissions and post‑marketing support. Design and maintain statistical datasets supporting multiple stakeholder groups (clinical development, outcomes research, safety evaluation). Collaborate with statistics and project stakeholders to ensure timely, high-quality deliverables. Serve as statistical programming point of contact and knowledge holder through the product lifecycle. Primary Activities Develop, validate, and implement analysis/report programming using global/TA standards, departmental SOPs, and good programming practices. Maintain and manage project plan, including resource forecasting. Coordinate activities of a global programming team (including outsource provider staff). Participate in departmental strategic initiative teams. Education Minimum Requirement BA/BS plus 5+ years SAS programming experience in a clinical trial environment. MS plus 3+ years SAS programming experience in a clinical trial environment. Required Skills/Experience Interpersonal, negotiation, collaboration; strong written/oral/presentation skills. Experience creating R&D analysis/reporting deliverables (data, analyses, tables, graphics, listings). Ability to independently complete project-level tasks and collaborate with stakeholders. SAS clinical trial programming expertise (data steps, procedures, SAS/MACRO, SAS/GRAPH) and systems/database expertise. Ability to design complex programming algorithms; understand analysis plans and statistical terminology. Familiarity with clinical data management; experience with CDISC and ADaM standards. Ensure process compliance and deliverable quality; strategic thinking and stakeholder requirement anticipation. Preferred Skills/Experience R programming for statistical modeling/analysis/visualization. Regulatory application submission experience (including electronic submission deliverables). Program consistency across protocols/projects; mentorship; cross‑cultural/geographic teamwork. Experience using global outsource partner staff; Microsoft Project (or similar) for planning. Process improvement; active professional society involvement. Application Instructions Apply via (deadline stated on posting). #J-18808-Ljbffr Scorpion Therapeutics