The role involves collaborating with clinical development staff to meet project timelines for statistical data analysis and reporting. The individual will generate statistical analysis datasets and outputs for study reports and integrated summaries. Responsibilities include assessing the quality and consistency of analysis data and performing cross-study analyses. The position requires automating study deliverables through the use of internal or written macros. Additionally, the role involves assisting in the submission of electronic data to regulatory agencies and contributing to the continuous improvement of the programming environment.

Candidates must possess either a Master's degree with 2 years of relevant experience or a Bachelor's degree with 4 years of relevant experience. Proficiency in SAS programming is required, along with knowledge of clinical trial study design and electronic data submission requirements. Excellent verbal, written, and interpersonal skills are necessary for the role. Preferred qualifications include a degree in Biostatistics or Computer Science, 5 or more years of pharmaceutical or CRO experience, and expertise in oncology, hematology, or cell therapy.