A company is looking for an Associate Director, Statistical Programming (Remote).
Key Responsibilities
Lead statistical programming teams and support the development, regulatory approval, and market acceptance of products
Design, develop, and implement technical solutions for integrating, analyzing, and reporting clinical data
Validate programming results from external vendors and independently develop, validate, troubleshoot, and maintain complex programs
Required Qualifications
Bachelor's degree with 12 years, Master's degree with 8 years, or PhD with 5 years of experience in Biostatistics or Statistics
At least 8 years of programming experience in the industry, including support of significant regulatory filings
Proficient knowledge of drug development processes, clinical trial methodology, and regulatory guidance
SAS programming experience in oncology studies
In-depth understanding of clinical data structure and relational databases
Director Statistical Programming • El Paso, Texas, United States