Match Score
Against your primary resumeLogin to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Protocol Intelligence
Data-driven signals on your job's competitivenessLog in to see why each signal reads the way it does.
Job Description
Structured overview of role & requirementsAbout This Role
Lead the programming, testing, and documentation of statistical programs for complex studies to produce tables, figures, and listings.
Plan, coordinate, and integrate databases from multiple studies or sources, including development and validation of new programming processes, macros, and applications.
Act as statistical team lead managing scope, budget, resource forecasts, and providing internal consultancy and training on advanced technical expertise.
Minimum Requirements
Master's degree in Computer Science or related field with 3 years relevant experience OR Bachelor's degree with 4 years relevant experience, or equivalent combination.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language programming.
Knowledge of statistics, programming, and clinical drug development processes.
Work Experience Required: 3-4 years depending on degree level.
Ideal Candidate Profile
Experienced in managing end-to-end statistical programming projects for complex clinical studies with leadership accountability.
Skilled in cross-study database integration and advanced SAS programming techniques including macro development.
Capable of independently consulting with clients internally and externally and managing study budgets and resource allocations.