Associate Director, Statistical Programmer

About the role

Statistical programming sits at the heart of clinical evidence generation — and in this role, you will be instrumental in turning complex data into the high-quality deliverables that advance medicines from development to patients. As a Statistical Programmer at the Senior or Principal level, you will contribute to and lead statistical programming activities across one or more clinical trials and global project sub-tasks within clinical development programs.

What you'll do

• Be instrumental in turning complex data into the high-quality deliverables that advance medicines from development to patients
• Contribute to and lead statistical programming activities across one or more clinical trials and global project sub-tasks within clinical development programs
• Coordinate programming workstreams, provide oversight of Contract Research Organization (CRO) activities, and ensure the timely
• Play an active role in advancing best practices and process improvements within the global Biostatistics function — sharing knowledge, guiding colleagues

What you need

• 8–14 yrs of experience
• Regulatory affairs
• CRO
• Communication
• Clinical research
• Any graduate