About this role
Primary Function / Primary Goals / Objectives: The Statistical Analyst will review table mockups, CRFs and edit check specifications; work with biostatisticians and clinical staff to generate data tables, figures and listings; write and document programs; perform ad hoc programming; and perform QC tasks.
Major Responsibilities: Responsible for implementing and maintaining the effectiveness of the quality system. - Perform QC of tables, presentations and reports. - Review CRFs, edit check specifications and table mock-ups. - Assist in creation of table mockups under supervision of statisticians or senior statistical analysts - Generate or validate table programs - Perform adhoc programming with assistance from statisticians or senior statistical analysts - Provide data listing or summary to Data Management for data cleaning - Document programs and specifications - Demonstrate knowledge of SAS data steps, procedures and macros - Be able to use and modify existing macros - Provide accurate and timely answers to routine questions - Communicate an understanding of basic clinical principles for his/her project and acts in accordance with those principles. - Inform supervisor or manager on important issues in a timely manner.
Education / Experience Required: BS or BA with 3-5 years or MS with 18 months of related work experience
Accountability / Scope: Position interacts with customers from clinical research. Effective communication with various levels of personnel is required regularly.
Problem Solving: Position communicates an understanding of clinical trial principles for assigned projects and acts in accordance with those principles; effectively and persuasively presents programming concepts to customers within the project team.