Senior SAS Programmer - Clinical Trials Lead

Parexel; United Kingdom; Remote; GBP 50,000 - 70,000; Full time

Job summary

A global biopharmaceutical services company is seeking a Senior Statistical Programmer in the UK. This role involves creating SAS programs, providing programming support for clinical trials, and ensuring the quality of deliverables while adhering to regulatory standards. The ideal candidate has a Bachelor's degree in a related field and at least 5 years of experience in clinical programming. Join us to make a significant impact in clinical development.

Qualifications

• Minimum of 5 years clinical/statistical programming experience in pharmaceutical clinical development.
• In-depth understanding of clinical data structure (e.g., CDISC standards).
• Demonstrated ability in handling and processing upstream data.

Responsibilities

• Create SAS programs for analysis datasets and outputs.
• Provide programming support for project teams.
• Review key planning documents for programming requirements.

Skills

SAS proficiency

Analytical programming

Biostatistics

Clinical data structure (CDISC)

Team collaboration

Education

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences

Tools

MS Office

XML

Pinnacle 21

Job description

A global biopharmaceutical services company is seeking a Senior Statistical Programmer in the UK. This role involves creating SAS programs, providing programming support for clinical trials, and ensuring the quality of deliverables while adhering to regulatory standards. The ideal candidate has a Bachelor's degree in a related field and at least 5 years of experience in clinical programming. Join us to make a significant impact in clinical development.