Principal Statistical Programmer, PKPD
About The Position
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. 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
Requirements
- 8+ years of statistical programming experience in the pharmaceutical or CRO environment.
- Prior experience working in an FSP engagement model preferred.
Nice To Haves
- Experience supporting Translational Medicine or Clinical Pharmacology groups.
- Familiarity with internal exploratory analysis and early-phase decision-making needs.
- Exposure to integrated summaries or pooled PK analyses across studies.
Responsibilities
- Expert-level SAS programming skills.
- Strong, hands-on experience with CDISC SDTM, ADaM and TLFs.
- Proven experience developing safety, PK, and PK/PD ADaM datasets.
- Experience supporting POPPK/popPD/Exposure Response(ER) dataset creation workflows.
- Solid understanding of early-phase clinical trial designs, including: Phase I / First-in-Human Crossover studies, Exposure–response analysis, PK parameter pooling.
- Demonstrated experience as a Lead Programmer or technical lead.
- Experience supporting regulatory submissions is required.
- Strong communication and stakeholder management skills.
- Ability to work independently while managing multiple priorities.
- Detail-oriented with a strong commitment to quality and timelines.
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Full-time
Career Level
Principal
Education Level
No Education Listed
