Senior Director, Statistical Programming

📋 Description

• Lead statistical programming strategy and ensure on-time, high-quality deliverables.
• Provide strategic and technical leadership for programming in clinical trials.
• Serve as senior CDISC expert (SDTM/ADaM) for submissions.
• Partner with Biometrics Lead to shape long-term strategy and resources.
• Drive SOPs, tools, and workflows to improve efficiency and quality.
• Oversee CROs/external vendors and governance for timely, quality work.

🎯 Requirements

• Deep expertise in statistical programming in biotech/pharma.
• Proven track record leading programming strategy in clinical development.
• Expert SAS programming and CDISC SDTM/ADaM for regulatory submissions.
• Experience managing CROs/vendors, governance, relationships.
• Proven leadership with mentoring and cross-functional influence.

🎁 Benefits

• 401(k) plan with 4% company match and immediate vesting.
• Medical, dental, and vision insurance for employees and families.
• Health and Dependent Care FSAs.
• Employee assistance program (EAP).
• Paid time off + company holidays; flexible schedule.
• Hybrid work arrangement: 2-3 days onsite in Lexington, MA with remote other days.