Associate Director, Data Validation Engineer

Job Summary

Leading clinical trial reporting activities, the full-time Associate Director, Data Validation Engineer will oversee the development of data listings and visualizations, ensuring high-quality data delivery for regulatory submissions while collaborating with various study teams in a remote capacity.

Key responsibilities:

• Provide expertise and leadership in clinical trial reporting for global development programs
• Drive strategy with preferred vendors to ensure compliance with regulations and standards
• Organize clinical trial reporting activities and collaborate with cross-functional teams on data quality checks and visualizations

Required qualifications:

• BS/BA in a health-related or technology-related field
• Minimum of 8 years of drug development experience, with at least 6 years in project management and leadership
• Experience in programming listings and visualizations using tools such as Veeva CDB and JReview
• Knowledge of clinical database systems and experience with programming languages like SQL, SAS, or Python
• Familiarity with FDA and ICH regulations and quality control principles related to clinical trial data