• Required Skills & Experience
• Technical Skills
• + •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
• Experience
• + •8+ years•of statistical programming experience in the pharmaceutical or CRO environment.

+ Demonstrated experience as a

• Lead Programmer
• or technical lead. + Prior experience working in an
• FSP engagement model
• preferred. + Experience supporting
• regulatory submissions
• is required.
• Soft Skills
• + Strong communication and stakeholder management skills. + Ability to work independently while managing multiple priorities. + Detail‑oriented with a strong commitment to quality and timelines.
• Preferred Qualifications
• + 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. 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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

https:

//jobs.iqvia.com/eoe 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. The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. 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. EEO Minorities/Females/Protected Veterans/Disabled