Greetings from IT Engagements

Position: Clinical SAS Programmer
Location: Pleasanton, CA Onsite

Skills :

Must have knowledge of Base SAS, SAS/STAT, SAS macros, and SAS/GRAPH. Experience in TLFs, Submissions etc

• Bachelor’s degree in Statistics, Mathematics, or Computer Science or in a related field.
• Minimum of 8 years Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer.
• Knowledge of SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS.
• Demonstrates extensive knowledge with industry standards.
• Excellent communication and interpersonal skills to effectively interface with others.

Duties:

• Generate analysis datasets, tables, figures, and listings to support the statistical analysis of clinical trials .data in support of regulatory submissions and publications.
• Generate SDTM domains, ADaM datasets, and Define.xml or Define.pdf files.
• Perform quality control for SAS programs and other study documents (e.g., presentations and reports).
• Maintain complete and auditable documentation of all programming activities.
• Review output across SAS programs to ensure consistency.
• Provide statistical programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.
• Assist in programming, testing, and documenting SAS global utility programs and tools in accordance with standards and validation procedures.
• Review CRFs, edit check specifications, and table mock-ups.
• May assist in creation of table, figure, or listing mockups under supervision of statisticians.
• Other duties as assigned.

Thank you

Job Type: Contract

Pay: Up to $70.00 per hour

Schedule:

• 8 hour shift
• Monday to Friday

Experience:

• clinical SAS: 6 years (Preferred)
• Macros: 4 years (Preferred)

Work Location: In person