Responsible for all statistical programming, data review reporting, and analytics development aspects of studies, projects, or project-level activities
Job Summary
Responsible for all statistical programming, data review reporting, and analytics development aspects of studies, projects, or project-level activities.
Acts as a key collaborator and strategic partner to ensure efficient drug development with timely, high-quality deliverables.
Ensures timely and quality development and validation of datasets and outputs for regulatory submissions, safety reports, publications, and post-marketing activities.
Matching Summary
Responsible for all statistical programming, data review reporting, and analytics development aspects of studies, projects, or project-level activities.
Skills & Requirements
Must-have
SAS for clinical trial data analysis
End-to-end study responsibility
CDISC data standards
R and other programming languages
AI/ML technologies
Nice-to-have
Cross-functional team collaboration
Knowledge sharing and innovation
Problem-solving expertise
Key Requirements
Minimum 6 years of experience with Graduation (MSc preferred)
Experience in development/review of critical study documents