Associate Director, Statistical Programming (LM)

Tasks

• Act as technical subject matter expert
• Deliver clinical study statistical programming
• Develop data standards and automation approaches
• Drive continuous improvement and best practices
• Lead and manage programming team
• Lead statistical programming protocol implementation
• Manage clinical programming compliance and quality
• Manage external partners and CROs
• Provide training and mentorship
• Recruit and develop team talent

Perks/Benefits

• Hybrid work model

Skills/Tech-stack

Automation | CDISC | Clinical trial | Data Standards | R | Risk Management | SAS | SAS Macros