IQVIA
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
Principal Statistical Programmer – Permanent Homebased
🔥 1 minute ago
Where this job comes from
Posted on IQVIA's careers page ↗, not through a job board
First seen by Remote Rocketship 1 minute ago
IQVIA
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
📋 Description
• Lead statistical programming activities across multiple clinical studies and programs • Serve as a Study Lead, providing oversight, mentorship, and technical guidance to programming teams • Develop, validate, and review analysis datasets, tables, listings, and figures using SAS and R • Drive programming standards, efficiencies, and process improvements across studies and therapeutic areas • Author and review programming specifications, validation plans, and study documentation • Ensure high-quality delivery of regulatory submission packages in compliance with industry standards • Collaborate with Biostatistics, Data Management, Clinical, and other cross-functional stakeholders to resolve data and programming issues • Support strategic initiatives through reusable programming tools and solutions
🎯 Requirements
• Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related field • Minimum 8+ years of statistical programming experience within the pharmaceutical, biotechnology, or CRO industry • At least 2+ years of experience as a Study Lead/Lead Programmer, or experience developing SAS/R solutions implemented across multiple studies, programs, or therapeutic areas • Intermediate/Advanced programming expertise in SAS (Base and Macro) and R • Strong knowledge of CDISC standards (SDTM, ADaM, Pinnacle 21) and regulatory submission requirements • Proven experience supporting efficacy analyses, statistical reporting, and regulatory deliverables • Experience developing and reviewing programming specifications and technical documentation • Strong understanding of clinical trial data, including study population, efficacy, safety, and PK/PD analyses • Demonstrated leadership, project management, and organizational skills, with the ability to manage multiple priorities • Excellent communication skills with experience collaborating across cross-functional teams and engaging with key stakeholders • Hands-on experience with R programming in a clinical development environment • Experience supporting global regulatory submissions (FDA, EMA, PMDA) • Previous experience working within an FSP model supporting pharmaceutical sponsors • Experience driving programming innovation, automation, and standardization initiatives
🏖️ Benefits
• Permanent homebased role • Mentorship and technical guidance opportunities • Opportunity to support strategic initiatives through reusable programming tools and solutions • Collaboration with global pharmaceutical clients and cross-functional teams
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