Senior Statistical Programmer & Study Lead – SAS/R

IQVIA Inc; Stockholms kommun; On-site; SEK 1,200,000 - 1,800,000; Full time

Job summary

IQVIA Inc. is seeking an experienced Principal Statistical Programmer to provide technical leadership across Phase I-IV clinical trials, driving high-quality programming solutions, regulatory submissions, and study-level strategy.

You will lead programming activities, mentor teams, develop and review TLFs with SAS and R, and ensure adherence to CDISC standards while collaborating with cross-functional stakeholders to enable successful submissions.

Qualifications

• Bachelor's or Master's degree in statistics, mathematics, computer science, life sciences, or a related field.
• Minimum 8+ years of statistical programming experience in pharma/biotech/CRO.
• At least 2+ years as Study Lead/Lead Programmer overseeing trials.
• Strong SAS (Base/Macro) and R skills with regulatory submission experience.
• Knowledge of CDISC standards (SDTM/ADaM) and regulatory requirements.

Responsibilities

• Lead statistical programming activities across multiple clinical studies.
• Serve as Study Lead, mentoring programming teams.
• Develop, validate, and review TLFs using SAS and R.
• Drive standards, efficiencies, and process improvements.
• Author programming specs, validation plans, and study documentation.
• Support regulatory submission packages in compliance with standards.
• Collaborate with cross-functional stakeholders to resolve data issues.
• Develop reusable programming tools and solutions.

Skills

Leadership

Cross-functional collaboration

Project management

Communication

Clinical trial data knowledge

Education

Bachelor's or Master's in Statistics / Mathematics / CS / Life Sciences

Tools

SAS Base / Macro

R programming

SDTM / ADaM

Pinnacle 21

Regulatory submissions

Job description

IQVIA Inc. is seeking an experienced Principal Statistical Programmer to provide technical leadership across Phase I-IV clinical trials, driving high-quality programming solutions, regulatory submissions, and study-level strategy.

You will lead programming activities, mentor teams, develop and review TLFs with SAS and R, and ensure adherence to CDISC standards while collaborating with cross-functional stakeholders to enable successful submissions.