Job Description
📋 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.
