Regeneron is seeking a Sr. Manager - Statistical Programming to lead statistical programming activities across multiple clinical programs, ensuring high-quality, compliant data outputs for regulatory submissions, integrated analyses, and clinical trial transparency.
Requirements
- Strong experience in statistical programming within clinical trials, including integrated analyses and regulatory submissions
- Deep understanding of CDISC standards (SDTM, ADaM, Define-XML) and regulatory requirements
- Proficiency in SAS programming, with additional exposure to R or Python considered beneficial
- Experience with tools such as Pinnacle 21 (P21) for validation and compliance checks
- Demonstrated ability to lead teams, manage multiple projects, and deliver results in a fast-paced environment
- Strong analytical, problem-solving, and troubleshooting skills
- Excellent communication and stakeholder management capabilities
- Ability to work effectively in a matrixed, global organization and collaborate cross-functionally
- High attention to detail with a focus on quality and compliance
Benefits
- Health and wellness programs
- 401(k) company match
- Family support benefits
- Equity awards
- Annual bonuses
- Paid time off
- Paid leaves (e.g., military and parental leave)