Associate Director of Statistical Programming - Remote

Overview

We are seeking an Associate Director of Statistical Programming to lead statistical programming activities for clinical trials, manage programming teams, and ensure high-quality data deliverables.

In Short

• Lead statistical programming for clinical studies.
• Oversee programming vendors and validate datasets.
• Collaborate with cross-functional teams.
• Develop statistical programming processes and standards.
• Mentor a team of programmers.
• Generate ad hoc analyses.
• Manage CROs and data vendors.
• Maintain knowledge of regulatory guidelines.
• Promote a psychologically safe environment.
• Travel up to 10% for company meetings.

Requirements

• Master’s Degree in Statistics or related field.
• 10+ years of clinical trial programming experience.
• Advanced SAS and R programming skills.
• Knowledge of CDISC standards.
• Excellent organizational and communication skills.
• Experience managing CROs.
• Strong leadership and growth mindset.
• Ability to work in a fast-paced environment.
• Knowledge of ICH and FDA guidelines.
• Experience in a remote virtual environment.

Benefits

• Great company culture based on C.O.R.E. values.
• Dynamic work environment with growth opportunities.
• Competitive compensation and benefits package.
• Flexible PTO.
• Company-wide shutdowns for work-life balance.
• Commitment to professional development.
• Regular in-person team meetings.