Senior Statistical Programmer - FSP

As a Senior Statistical Programmer at IQVIA, you will be responsible for planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs. This role involves providing internal consulting services, including specifications and user needs analysis for complex project or client requirements. You will work in a collaborative environment, utilizing cutting-edge technology to support clinical research studies across various therapeutic areas.

Key Responsibilities

• Study Implementation: Perform, plan, coordinate, and implement activities for complex clinical studies.
• Programming & Testing: Handle the programming, testing, and documentation of statistical programs used to create statistical tables, figures, and listings (TFLs).
• Analysis Datasets: Program analysis datasets (derived datasets) and transfer files for both internal and external clients.
• Quality Control: Execute quality control checks for source data and report data issues periodically to ensure accuracy and compliance.
• Specifications: Interpret project-level requirements and develop comprehensive programming specifications for complex studies.
• Technical Leadership: Act as a technical team lead for single complex studies or groups of studies, providing advanced technical expertise and bringing innovative solutions to Statistical Programming (SP) teams.
• Communication: Directly communicate with internal and client statisticians and clinical team members to ensure a shared understanding of requirements and project timelines.
• Project Management: Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
• Mentorship: Promote the use of established standards, SOPs, and best practices, and provide training and mentoring to other SP team members.

Requirements

• Bachelor's Degree in Mathematics, Computer Science, Statistics, or a related field.
• A minimum of 7 years of Statistical Programming experience specifically within the Life Science Industry.
• Strong experience in Efficacy analysis.
• Advanced knowledge of statistics, programming, and/or the clinical drug development process.
• Advanced proficiency in computing applications such as Base SAS, SAS Graph, and SAS Macro Language.
• Advanced knowledge of relevant Data Standards, including CDISC, ADaM, and SDTM.

Benefits

• Global exposure to diverse projects.
• Opportunity to work in various therapeutic areas.
• Collaborative and supportive team culture.
• Access to innovative, in-house technology.
• Clear career development and progression paths.
• Focus on work-life balance and overall well-being.