We are seeking a Principal ADS Program Lead to guide the technical strategy and operational execution across multiple clinical programs or an entire therapeutic area. The role leads a team of highly skilled programmers and junior leaders, ensuring the delivery of high-quality, regulatory-compliant analytical outputs.
Requirements
- Holding an advanced degree (Master's or PhD) in Data Science, Statistics, Computer Science, Biomedical Informatics, or a related field
- Minimum of 6 years of experience in pharmaceutical R&D or a regulated environment, with significant exposure to clinical development
- Demonstrated leadership of molecule-level analytical strategy or delivery across multiple studies
- Strong technical expertise in statistical programming (e.g., R, SAS), QC practices, and regulatory data standards (e.g., CDISC, ADaM, SDTM)
- Proven ability to manage complex timelines, collaborate across functions, and communicate analytical strategies effectively
Benefits
- 401k Matching
- Retirement Plan
- Generous Paid Time Off