Senior Statistical Programmer (m / w / d) - Fully homebased / remote

IQVIA; Bloemfontein; Remote; ZAR 600 000 - 800 000; Full time

Job summary

A leading company in analytics and clinical research is seeking an experienced Statistical Programmer. This remote role involves developing clinical study report materials, programming datasets, and mentoring team members. Candidates should have strong SAS skills and relevant degrees. Join to advance clinical trial statistical analysis with innovative technology.

Qualifications

• 5+ years in a Statistical Programmer role within CRO, Pharma, or Biotech.
• Expertise in ADaM, SDTM, and TLFs.

Responsibilities

• Import data from multiple sources.
• Perform quality control checks on source and reporting data.
• Program SDTM and ADaM datasets.

Skills

Analytical Skills

Problem-Solving

Organizational Skills

Communication Skills

Education

Master’s Degree in Biostatistics

Bachelor’s Degree in Statistics

Bachelor’s Degree in Mathematics

Bachelor’s Degree in Computer Science

Tools

SAS

Job description

IQVIA Statistical Programmer Role

IQVIA is seeking experienced statistical programmers proficient in SAS to develop clinical study report materials for regulatory submissions. This role involves end-to-end programming tasks within our DS3 environment (home-based), supporting various aspects of statistical programming.

Responsibilities

1. Import data from multiple sources
2. Perform quality control checks on source and reporting data
3. Interpret project requirements and develop programming specifications
4. Write code following Good Programming Practices
5. Program SDTM and ADaM datasets
6. Create statistical analysis tables, listings, and figures
7. Validate datasets and outputs against gate checks
8. Communicate effectively with statisticians and clinical teams
9. Adhere to standards, SOPs, and methodologies
10. Export data and report materials
11. Mentor and train team members

Join us to advance clinical trial statistical analysis with cutting-edge technology across global projects and therapeutic areas. Enjoy a collaborative, fast-paced environment with growth and mentoring opportunities to develop your career.

The Person

Candidates should hold a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, with strong programming experience.

Key Skills and Experience

• 5+ years in a Statistical Programmer role within CRO, Pharma, or Biotech industries, with expertise in ADaM, SDTM, and TLFs
• Proficiency in SAS programming
• Strong analytical, problem-solving, and organizational skills
• Excellent communication skills
• Knowledge of GCP and ICH guidelines
• Ability to lead programming tasks independently and manage timelines

We value curiosity, initiative, integrity, and the ability to build effective working relationships. This role is remote and not eligible for UK visa sponsorship.

IQVIA is a global leader in analytics, technology, and clinical research services, committed to advancing human health through innovative data science. Learn more at our website.