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Safety Group performs two major functions. One is using the Data Visualization tool to assist the clinical data review in near real time. Another function is to deliver regulatory agency required reports, e.g., Development Safety Update Reports (DSUR), Periodic Safety Update Reports (PSUR), Risk Management Plan (RMP) to PVE at the requested timeline. Job Functions: The ideal candidate should have background in both sciences and computer programming. S/he is detail oriented and is interested in SAS, Spotfire, Python, R programming and clinical trial knowledge. The internship will cover each individual project life cycle, programming activities, documentation. Job Responsibilities: • Learn and understand the basic knowledge of clinical trial. • Learn and familiar with individual project process life cycle. • Learn and familiar with standard data visualization or safety data Specification, table mockup, and other documents. • Learn/improve SAS, Spotfire, Python, R etc. programming • Help to review final output correction and inform lead programmer after completion. • Learn and document individual project activities to compliance with regulatory requirement. Candidate Qualifications: • Excellent detail oriented analytical, problem-solving skills. • Strong organizational, time-management, interpersonal and communication capabilities. • Knowledge of SAS, Spotfire, Python, R, familiar with Microsoft Office is plus. • Degree Major(s) preferred: Computer Science, Statistics/Biostatistics, Mathematics, other equivalent scientific field. • Ability to complete 10-12 consecutive weeks between May and September.
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