September 30
• Provides collaborative input and guidance to the design of SAS outputs to the client and internal teams to develop metrics, reconciliation reports, tools, listings and standard patient profiles • May support the development of complex proprietary patient profiles designed to facilitate efficient holistic data review & centralized monitoring, aggregate data review workbooks, metrics, projections, graphs and other data visualizations including the application of oncology disease assessment criteria, CTCAE criteria, etc. • Ensures on-time delivery, communicates the status of projects to internal teams and study • Develops, tests, and validates SAS programs to support client-related and cross-functional projects • Troubleshoots and resolves SAS program issues • Develops and maintains SAS programming validation documents • Participate in conducting demonstrations and trainings • Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to SAS programming activities • May provide leadership for cross-functional and organization-wide initiatives, where applicable • May train project team members • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues • Present software demonstrations/trainings, department/company training sessions, present at project meetings • May require some travel • May perform other duties as assigned
• Bachelor's degree or equivalent in local country or equivalent level of experience • Minimum of 3+ years of experience in clinical, scientific or healthcare discipline • Broad knowledge of drug, device and/or biologic development and effective data management practices • Base SAS®, SAS/STAT and SAS/ACCESS software • SAS Macro Language • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook • Excellent organizational and communication skills • Professional use of the English language; both written and oral • Experience in utilizing various clinical database management systems (EDC) • Experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), R, SQL • Oncology and/or Orphan Drug therapeutic experience
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