Job
Description
Roles and Responsibilities
Study design, Sample size estimation, and statistical write-up for protocol as per regulatory requirement.
Protocol inputs and Statistical Analysis Plan (SAP) for clinical trials and BA/BE studies.
Data management: Concatenating, Merging, Handling missing values, Reading raw data files, creating data structures, Handling data and programming errors, Accessing data, Appending data and managing data.
handling and coordinate with data management team for clinical data.
Design and write statistical sections for clinical trial protocols.