Associate Director Stat. 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 an Associate Director, Statistical Programmer, you will contribute to and lead statistical programming activities across one or more clinical trials and global projects within clinical drug 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 projects within clinical drug development programs
• Provide functional leadership for programming activities, coordinate and oversee work performed by CRO partners and internal programmers and ensure the timely and…
• Make an impact through your technical expertise, project leadership, and collaboration across teams
• Play an active role in advancing best practices and process improvements within the Global Biostatistics function — sharing knowledge, guiding colleagues

What you need

• 10–18 years in software engineering
• CRO
• Regulatory affairs
• Clinical research
• Any graduate