Associate Director of Stats Programming

About the role

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. This role supports our Electrophysiology business, working onsite in our Irvine, CA office, following a hybrid schedule.

Responsibilities

• Lead a team of SAS and R programmers in the Medical Devices Sector
• Ensure accurate and timely delivery of statistical deliverables for pre- and post-market global clinical trials across all Franchises
• Maintain and develop global SAS macro and R function libraries
• Collaborate with Data Management leadership to establish data and process standards
• Oversee vendor evaluations, selections, and contract management for studies involving outsourced programming
• Work with Clinical Data Science partners and leadership in Clinical Operations and Franchise to set priorities and develop project management plans for trial execution
• Oversee quality reviews of all programming deliverables
• Comply with all relevant laws, policies, and regulations

Requirements

• Bachelor’s degree in Statistics, Computer Science, or related field with at least 8 years of programming experience in clinical research within Medical Device or Pharmaceuticals
• At least 3 years of supervisory experience
• Advanced SAS certification preferred
• Strong proficiency in Base SAS, SAS/STAT, and SAS Macro language
• Advanced proficiency in R, including advanced R programming
• Experience with CDISC datasets, tables, listings, and figures

Qualifications

• Demonstrated ability to lead teams to deliver critical milestones
• Excellent verbal and written communication skills
• Leadership competencies including Connect, Shape, Lead, and Deliver

Skills

• Advanced Analytics
• Biostatistics
• Collaboration
• Compliance Management
• Courage
• Critical Thinking
• Data Privacy Standards
• Data Synthesis
• Data Visualization
• Developing Others
• Good Clinical Practice (GCP)
• Inclusive Leadership
• Leadership
• Program Management
• Quality Assurance (QA)
• Regulatory Affairs Management
• Standard Operating Procedure (SOP)
• Statistical Analysis Systems (SAS) Programming

Pay

The anticipated base pay range for this position is: $137,000.00 - $235,750.00

Schedule

This role works onsite in our Irvine, CA office, following a hybrid schedule.