**Job Description**

**Responsibilities:**

+ Support statistical programming activities for clinical trial data analysis.
+ Develop SAS programs to create and validate analysis datasets (ADaM) and summaries (TFLs) in support of Clinical Study Reports and regulatory submissions (FDA, EMA, etc.).
+ Collaborate with biostatisticians, project leads, and other stakeholders in ensuring project plans are executed efficiently with timely and high-quality deliverables.
+ Develop effective study and report programming and validation utilizing global CDISC, ICH, and Therapeutic Areas standards and following departmental SOPs and good programming practices.
+ Maintain and manage a project plan including resource forecasting. Coordinate activities of a global programming team. Participate in departmental strategic initiative teams.

**Requirements:**

+ Master’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Biomedical Enginee...