Senior Clinical Programmer (DM SAS)

Develop, validate, and maintain clinical programming software using tools like SAS, Medidata, Oracle products to support clinical trials deliverables.

Lead and manage clinical programming activities across multiple studies, coordinating resources and ensuring adherence to project timelines and quality standards.

Provide technical support, application administration, and subject matter expertise for clinical programming tools, including audit participation and budget monitoring.

Bachelor’s degree preferred or equivalent combination of education and experience.

Minimum 5+ years of experience in Clinical Programming.

Proficiency in SAS programming, listings programming, and macros; experience with study build and SAS mapping is preferred.

Ability to travel up to 25%; Good communication skills mandatory.

Experienced clinical programmer capable of managing multiple concurrent studies and coordinating with cross-functional teams in a dynamic environment.

Strong technical expertise in clinical data management tools (e.g., SAS, Oracle Inform, Medidata Rave) with leadership experience in clinical programming deliverables.

Demonstrated ability to handle sponsor interactions, participate in audits, and monitor project scope and budgets effectively.