A leading pharma company in California is seeking a new Statistical Programmer Consultant to provide programming support for clinical studies.

About the Opportunity:
- Shift: Day
- Schedule: Full-time
- Hours: 9am to 5pm
- Setting: Office/Lab
Responsibilities:
- Providing programming support for multiple projects/studies across various therapeutic areas
- Creating and reviewing annotated CRF to SDTM datasets
- Balancing conflicting priorities and promoting effective communication
- Functioning as a positive role model and collaborating with various departments
- Providing technical input into documents and developing data review tools
- Performing other duties, as needed
Qualifications:
- 1+ year of Clinical Trial Programming experience
- Master's Degree in Statistics, Computer Science, Mathematics, Engineering, or related discipline
- Advanced SAS programming skills; experience with R and S-Plus
- Experience with CDISC standards, including SDTM, ADaM
- Self-directed and technically strong with project management skills
- Excellent organizational skills
- Strong communication skills
Desired Qualifications:
- PhD in a related field
- SAS certification
