Senior Clinical Programmer (DM SAS)

Overview

Lead clinical programming and data management activities across multiple studies, using tools including SAS, Medidata Rave, and Oracle platforms. The role covers software development, validation, technical support, project coordination, and stakeholder communication.

What you'll do

• Design, write, validate, and maintain clinical programming software.
• Develop specifications, database configurations, edit checks, data processing setups, listings, and reports.
• Lead programming activities across three to ten concurrent studies.
• Review study and program-level deliverables for accuracy.
• Provide application administration, technical support, and second-tier help desk support.
• Manage project resources, scope, budgets, and change orders.
• Provide leadership, training, and guidance to department members.

What you'll need

• At least 5 years of clinical programming experience.
• Bachelor's degree preferred or equivalent education and experience.
• Experience with listings programming and creating macros.
• Experience with study build and SAS mapping.
• Ability to manage multiple priorities in a dynamic environment.
• Excellent written and spoken communication skills.
• Proficiency with Microsoft Office, email, and voicemail.

Nice to have

• CDISC, external/vendor data mapping, and DIA experience.
• Base and Advanced SAS certification.
• Experience with PL/SQL, SAS, C#, or VB.
• Experience working in a matrix-structured environment.

Details

• Location: Hyderabad, India.
• Work mode: Hybrid.
• Travel: Up to 25% as necessary.