Responsibilities:
- Develop targeted, study-specific SDTM and ADaM dataset checks
- Perform independent QC, from raw data to ADaM, of primary and key secondary endpoints
- Deliver programming results for ad-hoc analysis requests
- Collaborate with data management and programming team to ensure appropriate data collection and reporting
- Participate in study team meetings and support statistician operational activities
- Assist in identifying, developing, and implementing departmental standards, applications, processes, and training
Requirements:
- Masterβs degree in Biostatistics/Statistics
- Basic understanding of clinical trials
- Working knowledge of SAS (complex data manipulation and basic analysis procedures) or certifications for SAS programming
- Excellent verbal and written communication skills
Preferred:
- Familiarity with CDISC standards; derivation of SDTM and ADaM specifications
- Simulations and sample size calculation
- Proficiency in R
- CRO experience
Benefits/Compensation:
- California pay range: $90,000 USD - $135,000 USD
- Competitive salaries and an excellent benefit package
Application instructions:
- Candidates must have current, valid authorization to work in the country where this role is located.