Lead Statistical Programmer for Complex Studies

IQVIA; España; Hybrid; EUR 85,000 - 125,000; Full time

Job summary

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical leadership across complex studies. You will plan and coordinate integrated programming solutions, develop specifications, and act as internal consultant for client requirements.

You will lead programming quality controls, mentor SP team members, and collaborate with statisticians and clinical teams to ensure timely, compliant deliverables.

Qualifications

• Bachelor's Degree in Maths, Computer science, Statistics, or related field
• 7+ years’ Statistical Programming experience within the Life Science Industry
• Strong Efficacy experience
• Advanced knowledge of statistics, programming and/or clinical drug development process
• Advanced knowledge of computing applications such as R, SAS, SAS Graph and SAS Macro Language
• Advanced knowledge of relevant Data Standards (CDISC/ADaM/SDTM)

Responsibilities

• Programming, testing, and documentation of statistical programs for tables, figures, and listings
• The programming of analysis datasets (derived datasets) and transfer files for clients
• Quality control checks for source data and reporting data issues regularly
• Interpret project requirements and develop programming specifications for complex studies
• Provide advanced technical expertise and project solutions to SP teams
• Lead technical work for single complex studies or groups of studies
• Communicate with internal and client statisticians and clinical teams on requirements and timelines
• Estimate scope, manage resources, and negotiate project timelines
• Promote use of established standards, SOPs, and best practices
• Provide training and mentoring to SP team members

Job description

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical leadership across complex studies. You will plan and coordinate integrated programming solutions, develop specifications, and act as internal consultant for client requirements.

You will lead programming quality controls, mentor SP team members, and collaborate with statisticians and clinical teams to ensure timely, compliant deliverables.