Associate Director – Statistical Programming

🔥 2 minutes ago

🇺🇸 United States – Remote

💵 $153k - $268.4k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Provide strategic and technical leadership for statistical programming activities across one or more therapeutic areas • Establish and maintain statistical reporting standards • Drive efficient, high-quality programming processes • Ensure compliance with CDISC and regulatory requirements • Support clinical development planning and execution across multiple indications • Lead statistical programming activities in a team-based environment aligned with business priorities, study objectives, and program timelines • Collaborate with cross-functional teams on clinical study planning and execution • Ensure accurate, consistent, and timely data reporting • Ensure quality and timeliness of statistical analysis, reporting, and regulatory submission deliverables • Promote best practices in programming environments, technology, and programming skillsets • Establish and maintain resource management and planning • Manage and mentor statistical programming and data analytics team members through guidance, training, feedback, and technical oversight • Support regulatory submission and inspection readiness • Manage and collaborate with CROs, overseeing programming activities and adherence to timelines and quality expectations

🎯 Requirements

• Master’s degree in Statistics, Mathematics, Computer Science, or a related discipline with 10+ years of SAS programming experience in a pharmaceutical, biotech, or CRO setting; OR Bachelor’s degree in those fields with 15+ years of SAS programming experience in a pharmaceutical, biotech, or CRO setting • Experience across both early and late phase/registrational trials • Strong experience with reporting processes, regulatory requirements, and the software development life cycle • Expertise in SAS programming • Hands-on experience with CDISC standards, including SDTM and ADaM • Experience programming raw data from different EDC and eCOA sources • Knowledge of R or Python • Strong written and verbal communication skills • Ability to work effectively in a cross-functional, matrixed environment and proactively influence teams • Demonstrated leadership experience, including collaborating with peers, overseeing and guiding colleagues, and driving business impact • Curiosity and passion for the work • Ability to embrace ambiguity and adopt new practices and technologies • Adaptive problem-solving ability • Technical depth and growth mindset • Interest in innovation, artificial intelligence, and digital technologies

🏖️ Benefits

• Company bonus depending in part on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • Prescription drug benefits • Healthcare and dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Employee assistance program • Fitness benefits • Employee clubs and activities • Infrequent travel under 10%