Clinical SAS Programmer

Artech Information System LLC; South San Francisco (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

A reputable workforce solutions company is seeking a SAS Programmer for clinical trial analysis in South San Francisco, California. This role involves performing SAS programming, ensuring compliance with sponsor requirements, and collaborating with Biostatistics and Data Management. Ideal candidates should have strong SAS programming skills and effective time management abilities. This position is expected to last 18 months and offers an opportunity to engage in impactful clinical projects.

Qualifications

• Strong SAS programming expertise is required.
• Effective time management skills are essential.

Responsibilities

• Perform SAS programming for clinical trial analysis and reporting.
• Ensure activities meet sponsor requirements.
• Collaborate with Biostatistics and Data Management departments.

Skills

SAS programming expertise

Time management

Job description

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada.

Job Description

Duration: 18 Months

Job Description:

• Performs all SAS programming required for clinical trial analysis and reporting.
• Ensures that activities and processes performed are conducted according to sponsor requirements.
• Works closely with the Biostatistics and Data Management departments on various clinical projects. Leads programming efforts for large complex studies. Requires time management skills, and strong SAS programming expertise.
• Reviews case report form (CRF) design. Designs and/or reviews database structure.
• Writes edit checks from the Data Cleaning Plan (DCP) specifications.
• Creates derived-analysis datasets. Executes analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under the guidance of the project statistician.
• Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses.