Key ResponsibilitiesDevelop and validate complexanalysis datasets (ADaM)andTFLsusing SAS.Write and reviewprogramming specificationsand supporting documentation.Createstandard macrosand tools to improve efficiency.Serve as aproject lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members.Communicate with clients as thekey programming contact, including delivering outputs and managing feedback.ConductSAS code review, track issues, and ensure quality standards are met.Archive all programming deliverables and documentation per SOPs.Mentor team members and support their technical and career development.Ensure compliance withICH-GCP, CDISC standards, and company SOPs.RequirementsBachelor's degree or abovein Statistics, Mathematics, Computer Science, or related field.5+ years of SAS programming experiencein pharmaceutical or CRO environments.Strong knowledge ofclinical trials ,statistical methods, andregulatory requirements .Proven experienceleading programming projectsand mentoring team members.Excellentcommunication skillsand experience working with global teams and clients.Proficient inSAS software .#J-18808-Ljbffr

📌 Senior Statistical Analyst Ii (Winnipeg)
🏢 Bilinguallink
📍 Winnipeg