Lead Statistical Programmer - Clinical Trials & CDISC

Cytel; Greater London; On-site; GBP 70,000 - 90,000; Full time

Job summary

A global pharmaceutical company is seeking a Principal Statistical Programmer to work embedded within a major client. The role focuses on delivering high-quality statistical programming, managing CRO deliverables, and ensuring adherence to FDA regulations. Ideal candidates will have a Bachelor's degree and over 7 years of experience in clinical development, with excellent skills in SAS and communication. This is an opportunity to join a team at the forefront of patient treatment innovation, with a strong emphasis on training and development.

Benefits

Training and development support

Opportunity for autonomy in work

Qualifications

• 7+ years of experience as a Statistical Programmer in Biotech/Pharma.
• Expertise in CDISC standards (SDTM, ADaM, Define.xml).
• Experience with regulatory submissions and FDA interactions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, and reviewer’s guides.
• Develop SAS programs for datasets, listings, and tables.
• Oversee CRO programming deliverables to ensure quality.

Skills

SAS programming

Statistical analysis

Communication skills

Leadership skills

FDA regulations knowledge

Education

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

Tools

R

Python

Unix/Linux

Job description

A global pharmaceutical company is seeking a Principal Statistical Programmer to work embedded within a major client. The role focuses on delivering high-quality statistical programming, managing CRO deliverables, and ensuring adherence to FDA regulations. Ideal candidates will have a Bachelor's degree and over 7 years of experience in clinical development, with excellent skills in SAS and communication. This is an opportunity to join a team at the forefront of patient treatment innovation, with a strong emphasis on training and development.