About the job
Role & Responsibilities
As a Clinical Programmer II at Syneos Health, you will leverage your expertise in Oracle RDC, Oracle Inform, Medidata Rave, SAS, and other relevant tools to design, develop, validate, and maintain software solutions that meet project specifications efficiently. You will be responsible for:
- Producing and maintaining essential documentation, including specifications, coding, and validation processes in support of annotated Case Report Forms (CRFs), database creation, coding configurations, edit check procedures, import/export setups, listings, and custom reports.
- Collaborating with project teams to coordinate and lead clinical programming activities. You'll actively participate in meetings, contribute to discussions, apply analytical problem-solving techniques, focus on deliverables, and provide constructive feedback. You’ll also keep project management informed of any issues that could affect timelines, scope, or budgets, escalating potential challenges promptly.
- Ensuring the quality of deliverables by reviewing study-level core outputs for accuracy and supporting sponsor audits as needed.
- Reviewing and providing insights on study budgets while monitoring the scope of work against actual deliverables, alerting management to any potential change orders.

