Description

You will execute statistical programming tasks for clinical trials data using SAS software systems.

This role is on-site.

Responsibilities

• Apply statistical programming techniques to manage and analyze clinical trial datasets.
• Lead technical tasks effectively within a team environment.
• Communicate technical findings and project progress clearly to stakeholders.
• Perform additional duties as requested to support project goals.

Required Skills

• 6+ years of programming experience specifically using clinical trials data.
• 6+ years of experience in SAS software systems.
• Expertise in SAS Statistical Programming.
• Experience with clinical trials data management.
• SAS Certification.
• CDISC training.
• Knowledge of multiple hardware platforms and various software environments.
• Four-year degree in a scientific discipline.

Key Skills

Education

Any Graduate