As a Senior Statistical Programmer, you will work fully embedded within a pharmaceutical client, leveraging your advanced SAS programming skills and proficiency in CDISC standards to support or lead clinical trials. This role can be performed as fully remote.
Requirements
- Performing data manipulation, analysis and reporting of clinical trial data
- Generating and validating SDTM and ADaM datasets/analysis files
- Production and QC/validation programming
- Generating complex ad-hoc reports
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with internal cross-functional teams and client
- Performing lead duties when called upon
- Serving as team player
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Visa Sponsorship
- Four Day Work Week
- Generous Parental Leave
- Tuition Reimbursement
- Relocation Assistance
