Director, Analysis Oversight Lead RWE: Inflammation

Position Summary Oversight of timeliness and quality of analysis results supporting the CDS‑RWE book of work for the Inflammation therapeutic area (TA). Reports to the CDS‑RWE TA Head; partners with scientific leads to implement strategies that deliver on portfolio priorities. Primary point of contact for study/analysis vendors and service vendors; responsible for planning, execution, and quality acceptance of analysis deliverables. Key Responsibilities Track, prioritize, and manage execution of analysis deliverables across the TA portfolio. Partner on data strategy and advanced analytical tools/methods for the TA portfolio. Manage vendor performance and escalation of risks impacting the TA portfolio. Oversee vendor plans, performance, and quality checks for programming, analysis, and other deliverables. Provide end-to-end oversight to ensure timely, high-quality completion aligned to TA priorities, with proactive risk identification/mitigation. Ensure translation of observational research protocols and analysis requirements into specifications/deliverables by vendors/service providers. Monitor/review quality of deliverables (specifications, programs, cohorts, feasibility results, analysis results, publications/abstracts, other outputs). Ensure locking or archiving of deliverables/outputs as appropriate. Monitor utilization and coordinate assignment of analyses to vendors/service providers. Serve as escalation point for quality, scope, and timeliness issues. Maintain regular communication with vendors/service providers to meet priorities/milestones. Ensure onboarding of vendors/service providers to tools, environments, and access to observational data. Identify/document process improvements (optimization, increased standardization, etc.). Collaborate with other TA oversight roles for uniformity/consistency. Collaborate with Gilead Data Office on awareness/training for licensed observational datasets. Qualifications Basic qualifications: Bachelor’s degree and 12+ years relevant experience; or Master’s degree and 10+ years relevant experience; or PhD and 8+ years relevant experience. 5+ years as a data scientist/data analyst generating analysis deliverables for observational research. BS required; MS or more advanced degree preferred in Computer Science, Data Science, Biostatistics, Epidemiology, or equivalent. Hands‑on experience with primary and real‑world data using multiple programming tools (e.g., SAS, R) in GxP‑compliant environments. Demonstrated experience leading/managing programmers and data analysts in a matrixed environment. Ability to review programs and outputs for quality, completeness, and best practices. Ability to communicate scope/requirements/standards; communicate and interpret analysis results. Strong data‑driven problem‑solving; cross‑functional collaboration with internal teams and vendor resources. Strong written and verbal communication. Preferred: understanding of RWE regulatory landscape; experience with international datasets and/or Common Data Models (e.g., OMOP). People Leader Accountabilities Create Inclusion; Develop Talent; Empower Teams. Benefits Salary range: $205,615.00 – $266,090.00. May be eligible for discretionary annual bonus, discretionary stock‑based long‑term incentives (eligibility varies), paid time off, and benefits package. Benefits include company‑sponsored medical, dental, vision, and life insurance plans. #J-18808-Ljbffr Scorpion Therapeutics