Clinical Data Scientist

March 26

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DRT Strategies

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Driving Resolution Together

Agile IT Management • Health Information Management • Portfolio • Program & Project Management • Financial Transformation

201 - 500

Description

• Support the Office of New Drugs within FDA’s Center for Drug Evaluation and Research (CDER) • Responsible for conducting safety data analyses and generating scientific reports • Collaborate with FDA stakeholders and clinical review teams

Requirements

• Minimum of 3 years professional experience • Technical proficiency in R programming • Strong analytical and statistical skills • PharmD or PhD in related STEM disciplines

Benefits

• Remote working status • Teleworking from home most of the time • Leveraging video conferencing and virtual productivity tools