Works highly independent and performs critical assessments in collaboration with study teams or other departments to determine best approaches to manipulate subject data
Reviews subject data from multiple sources with a data analytic mindset, capable of identifying trends, risks, gaps and areas for optimization as the subject data and the trial develops
Prepares and analyzes clinical trial patient datasets
Provides concise and clear updates to study teams and other key stakeholders after processing and reviewing subject data
Generates a thorough understanding of protocol schedule of events, EDC, Systems, Contracts, budgets and/or payment terms
Requirements
Bachelor's degree in life science-related fields, Engineering, Biostatistics and/or Programming or related fields/degrees