Job Summary
A company is looking for a Director of Statistical Programming.
Key Responsibilities:
- Develop and implement statistical programming strategies for clinical trials
- Oversee the creation and validation of CDISC-compliant datasets
- Direct the development of tables, listings, and figures for clinical study reports and regulatory submissions
Required Qualifications:
- MS Degree in Biostatistics, Statistics, or a related field with 8-10+ years of experience in statistical programming
- Extensive experience with CDISC standards and their application in clinical studies
- Strong proficiency in SAS programming and regulatory requirements for submissions
- Experience in preparing and reviewing key documents for regulatory submissions
- Proficiency in electronic data capture systems and clinical data management processes
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