Senior Statistical Programmer

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The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA is experienced in submissions for all major regions. They collaborate with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing to drive efficiency and accountability.

IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through clinical trials. It serves as the bridge between data capture and reporting.

We have one of the largest Biostatistics departments in the industry, with around 1,100+ staff, engaging industry-leading resources and expertise across all study phases and therapeutic areas.

Job Overview:

As a Senior Statistical Programmer, you will provide technical expertise to develop process methodologies for the department to meet internal and external client needs. You will plan and coordinate the development of integrated programming solutions for the full spectrum of statistical programming needs. Additionally, you will offer technical leadership and internal consulting, including specifications and user needs analysis for complex projects or client requirements.

Key Responsibilities:

1. Perform, plan, coordinate, and implement programming, testing, and documentation of statistical programs for creating tables, figures, and listings.
2. Program analysis datasets (derived datasets) and transfer files for clients.
3. Conduct quality control checks on source data and report data issues periodically.
4. Interpret project requirements and develop programming specifications for complex studies.
5. Provide advanced technical expertise in collaboration with clients and internal teams, bringing project solutions for complex studies.
6. Lead technical aspects for single or multiple complex studies.
7. Communicate with statisticians and clinical team members to ensure understanding of requirements and timelines.
8. Estimate scope of work, manage resources, and negotiate project timelines.
9. Train and mentor team members.

Requirements:

• 5+ years of Statistical Programming experience in the Life Sciences industry.
• BSc or MSc in Biostatistics or a related field.
• Experience with SAS Base, SAS Graph, and SAS Macros.
• Ability to implement advanced statistical procedures as specified by Biostatisticians.
• Excellent knowledge of CDISC standards (SDTM and ADaM).
• Understanding of relational database components and theory.
• Strong application development skills.
• Deep understanding of clinical trial data, data manipulation, analysis, and reporting.
• Ability to manage multiple projects, plan, organize, and prioritize.
• Experience leading technical teams and client engagement.
• Knowledge of GCP and ICH guidelines.

Join IQVIA to see where your skills can take you:

• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive environment
• Access to innovative technology
• Career development opportunities
• Work-life balance and well-being focus

Unleash your potential! Our culture of innovation and collaboration helps improve health worldwide by harnessing data, analytics, and healthcare expertise. Learn more at IQVIA.