Independently reviews whole protocol and interfaces with clinicians and other functions to understand study requirements and study design elements including sample size calculations, analysis methods, study durations etc. for multiple studies.
Develops and/or reviews statistical documents for multiple clinical trials, including SAPs, TLG shells and specifications of variable derivation. Support clinical trial related publications.
Independently provides statistical and validation support for analysis datasets, statistical tables, figures and listings. Performs and validates statistical analysis. Independently reviews CSRs and performs data interpretation.
Works with the internal/CRO statisticians and programmers to ensure the quality of CRO deliverables and on QA of data outputs.
Functions as lead statistician in global registration trials and manages all related statistical activities.
Leads preparation of inputs for regulatory documents and helps to prepare for meetings with health authorities. Leads preparation of responses to health authorities including identification and execution of new analysis required for responses.
Manages contract statisticians in the group. Provides mentoring and oversees assigned work.
Job Type: Full-time