Job Description
**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...
**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...
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