![Building A Digital PR Strategy: 10 Essential Steps for Beginners [With Examples]](https://buzzsumo.com/wp-content/uploads/2023/09/Building-A-Digital-PR-Strategy-10-Essential-Steps-for-Beginners-With-Examples-bblog-masthead.jpg)
![How One Brand Solved the Marketing Attribution Puzzle [Video]](https://contentmarketinginstitute.com/wp-content/uploads/2025/03/marketing-attribution-model-600x338.png?#)
Statistical Programming Associate Director
A company is looking for an Associate Director, Evidence Generation Statistical Programming. Key Responsibilities Support project leads on outsourced programming activities and ensure effective vendor programming implementation Provide hands-on statistical programming support for regulatory submissions and develop submission data packages Develop and maintain programming standards and tools to enhance programming efficiency and quality Required Qualifications Bachelor's degree in a science or technical field preferred; Master's degree preferred 10+ years of experience in the pharmaceutical industry or CROs supporting statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree Experience with SAS macro and/or system utility development preferred Advanced knowledge of CDISC SDTM and ADaM, and their implementation in clinical trials analysis preferred Understanding of statistical concepts and advanced statistical methods using SAS and R preferred
A company is looking for an Associate Director, Evidence Generation Statistical Programming.
Key Responsibilities
Support project leads on outsourced programming activities and ensure effective vendor programming implementation
Provide hands-on statistical programming support for regulatory submissions and develop submission data packages
Develop and maintain programming standards and tools to enhance programming efficiency and quality
Required Qualifications
Bachelor's degree in a science or technical field preferred; Master's degree preferred
10+ years of experience in the pharmaceutical industry or CROs supporting statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree
Experience with SAS macro and/or system utility development preferred
Advanced knowledge of CDISC SDTM and ADaM, and their implementation in clinical trials analysis preferred
Understanding of statistical concepts and advanced statistical methods using SAS and R preferred