Overview
Lead clinical programming activities for Rave studies, supporting database builds, edit checks, migrations, custom functions, validation, and related clinical data-management deliverables.
What you'll do
- Design, write, validate, and maintain clinical programming software using Rave and related tools.
- Develop specifications, database configurations, edit checks, imports, exports, listings, and custom reports.
- Lead programming activities across three to ten concurrent studies.
- Coordinate project teams, resources, deliverables, scope, budgets, and change orders.
- Provide application administration, technical support, system integration, updates, and user acceptance testing.
- Review deliverables, support audits, monitor system issues, and provide second-tier help desk support.
- Train and guide department members and collaborate with sponsors and internal teams.
What you'll need
- Five to eight years of clinical programming experience.
- End-to-end clinical programming experience in Rave.
- Experience with study and database builds, eCRF builds, edit checks, migrations, and custom functions.
- At least two years of custom function experience.
- Study-leading experience, including amendments and publishing checks and migrations.
- Bachelor’s degree preferred or an equivalent combination of education and experience.
- Strong communication, analytical, prioritization, and customer-management skills.
Nice to have
- Protocol interpretation experience.
- Experience in a matrix-structured environment.
- Programming experience with PL/SQL, SAS, C#, or VB.
Details
- Location: Hyderabad, India.
- Work mode: Hybrid.
- Travel: Up to 25% as necessary.
Read the full description and apply on the company’s own careers page.
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