Lead Statistical Programmer for Global Clinical Trials

Cytel; South Africa; On-site; ZAR 1,135,073 - 1,459,380; Full time

Job summary

Cytel is looking for a Principal Statistical Programmer to join its team in South Africa. In this role, you will work closely with a leading pharmaceutical client to generate statistical datasets and reports for clinical trials. You'll oversee CRO programmers and ensure the delivery of high-quality statistical programming results.

With a minimum of 5 years of experience in statistical programming and strong skills in SAS and CDISC standards, you will have the opportunity to contribute actively to the drug development process.

Qualifications

• 5+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team.
• Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities.
• Must be able to work independently.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, and guides for multiple studies.
• Develop SAS/R programs for datasets and complex listings.
• Deliver high-quality statistical programming results.
• Oversee CRO's statistical programming deliverables.
• Support the preparation of clinical study reports and regulatory submissions.

Skills

SAS programming expertise

Statistical programming procedures

CDISC standards knowledge

Exceptional communication skills

Leadership skills

Education

Bachelor's degree in computer science, data science, mathematics, or statistics

Advanced degree preferred

Tools

SAS

R

Job description

Cytel is looking for a Principal Statistical Programmer to join its team in South Africa. In this role, you will work closely with a leading pharmaceutical client to generate statistical datasets and reports for clinical trials. You'll oversee CRO programmers and ensure the delivery of high-quality statistical programming results.

With a minimum of 5 years of experience in statistical programming and strong skills in SAS and CDISC standards, you will have the opportunity to contribute actively to the drug development process.