Senior Statistical Programmer

• Contribute to or lead statistical programming activities for Phase I to IV clinical trials.
• Develop and validate datasets, tables, listings, and figures (TFLs) according to

specifications.

• Build and maintain effective working relationships with cross-functional teams (e.g.,

biostatistics, data management, clinical teams).

• Participate in team meetings and communicate programming progress and issues.
• Adhere to company, departmental, and industry standards (e.g., CDISC SDTM/ADaM, GCP).
• Ensure audit readiness and compliance with regulatory requirements.
• Review or develop programming specifications as part of statistical analysis plans.
• Participate in or lead the review of eCRFs and data structures.
• Ensure accuracy, reliability, and quality of statistical analysis results.
• Perform quality control checks on deliverables.
• Use SAS and other statistical programming tools (R and/or Python) effectively.
• Attend functional meetings and training sessions to enhance skills and knowledge.
• (At senior levels) Mentor and guide junior programmers.
• Contribute to process improvement, standardization, and non-clinical initiatives.

Unique Key Activities

• Lead programming for studies or project-level activities.
• Coordinate other programmers from the study or project.
• Represent programming in Clinical Trial Teams (CTTs), if performing the TP role.
• Provide input into programming solutions and project-level standards.
• Ensure quality and timely deliverables for all study level milestones like DMCs, IAs,

Publications, CSRs, submissions etc.

• Mentor junior programmers and contribute to process improvements

Experience/Professional Requirements

• Ideally 6-10 years of experience.
• Proven ability to deliver quality outputs and coordinate teams.
• Strong knowledge of CDISC and regulatory frameworks.
• Good understanding of regulatory requirements (e.g., GCP, ICH, etc.).
• Proficiency in R programming may be considered.
• Excellent communication and collaboration skills

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.