Senior Statistical Programmer - Pharmacometrics (Clinical Trials)

About the role

iQVIA is looking for a Senior Statistical Programmer in pharmacometrics (PM) support for clinical trials. The role is 100% home-based and dedicated to a single sponsor. The Principal Stat Programmer ensures the accuracy and integrity of statistical programming across clinical projects, develops and validates complex datasets and outputs, mentors junior programmers and contributes to improving programming workflows and standards.

Key responsibilities

• Develop and validate complex datasets and outputs using SAS programming, in line with CDISC standards such as ADaM and SDTM models.
• Collaborate with cross-functional teams to optimise statistical programming processes and improve efficiency and accuracy.
• Provide technical guidance on statistical methodologies to support clinical trial projects and departments.
• Mentor and guide junior programmers and foster their development.
• Contribute to continuous improvement of programming workflows and departmental standards, and ensure high-quality deliverables.
• Lead initiatives to improve programming tools and techniques, and partner with leadership to align programming objectives with organisational goals.

Required profile

• Bachelor's degree in Statistics, Computer Science or a related field.
• 2+ years working with efficacy analysis (ADaM datasets and TLFs) and/or 4+ years on ADaM statistical programming on clinical trials.
• Advanced English, written and spoken, tested during the interview; native language required (Spanish or Portuguese).
• Ability to lead and manage programming teams, adhere to standards and mentor others.
• Strong confidentiality, project management, problem-solving and communication skills.

Required skills

• Hands-on proficiency in R (mandatory)
• SAS programming
• CDISC standards, ADaM and SDTM models