Responsible for all statistical programming, data review reporting, and analytics development aspects of studies or projects, acting as a key collaborator to ensure efficient drug development
Job Summary
Responsible for all statistical programming, data review reporting, and analytics development aspects of studies or projects, acting as a key collaborator to ensure efficient drug development.
Leads statistical programming activities, makes strategic decisions at study or project level, and may act as a functional manager for local associates.
Ensures timely and quality development and validation of datasets and outputs for regulatory submissions, safety reports, publications, and post-marketing activities, while also generating innovative ideas.
Matching Summary
Responsible for all statistical programming, data review reporting, and analytics development aspects of studies or projects, acting as a key collaborator to ensure efficient drug development.
Skills & Requirements
Must-have
SAS for clinical trial data
CDISC data standards
Regulatory submissions and reporting
Nice-to-have
AI/ML technologies
R and other programming languages
Innovative project leadership
Key Requirements
Minimum 5 years experience with Graduation (MSc preferred)
End-to-end study responsibility as Trial Programmer
Experience with critical study documents development/review
Proficiency in SAS for clinical trial data analysis