Contract SAS Programmer for Clinical Trials (IVD/Pharma)

Beaufort; United States; On-site; USD 90,000 - 120,000; Full time

Job summary

Beaufort CRO is seeking an experienced Statistical Programmer for contract work supporting one or more life science client projects, including in vitro diagnostic, medical device and pharmaceutical studies. The role focuses on SAAS programming and analysis and requires strong SAS skills.

You will develop analysis datasets, run analyses per the SAP, document results, and help prepare CSR tables, listings and figures.

Qualifications

• Bachelor's degree required.
• 5+ years of statistical programming experience.
• Experience with SAS and clinical trial data.

Responsibilities

• Review protocols, SAPs, and programming plans.
• Create analysis datasets and perform SAS analyses.
• Validate analyses and incorporate client changes.
• Prepare final reports for CSR and archive documentation.

Skills

SAS programming

Industry standards

Clinical trial data

Education

Bachelor's degree

Job description

Beaufort CRO is seeking an experienced Statistical Programmer for contract work supporting one or more life science client projects, including in vitro diagnostic, medical device and pharmaceutical studies. The role focuses on SAAS programming and analysis and requires strong SAS skills.

You will develop analysis datasets, run analyses per the SAP, document results, and help prepare CSR tables, listings and figures.