Senior DM-SAS Clinical Programmer Hybrid (Serbia)

Principal Clinical Programmer (DM SAS) - Serbia, hybrid

Syneos Health is a leading fully integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum.

Job Responsibilities

• Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software following standard development procedures; generates documentation for specifications, CRFs, database creation, coding configuration, edit checks, imports, exports, listings, and reports.
• Serves on project teams to coordinate and lead development activities, attends meetings, provides analytical solutions, keeps project managers informed on issues impacting dates, scope, or budget, escalates problems, and balances tasks.
• Provides technology support to clinical programming staff and other teams, including application administration and technical support for core packages (Oracle Inform, MDSOL Rave, Oracle RDC, SAS, etc.) and supplemental packages.
• Ensures high quality deliverables by senior review of study level deliveries, attends sponsor audits, and assists with ongoing audits.
• Reviews budgets, monitors work scope, alerts management to change orders, and manages change order execution.
• Monitors application workflow, system errors and performance, and provides second tier help desk support.
• Performs system integration, updates, and user acceptance testing.
• Provides leadership, training, guidance, and support to other department members; collaborates with clients, peers, and project teams to clarify specifications.
• Participates in project meetings and departmental reviews, attends Quick Start Camps as lead clinical programmer for assigned studies.
• Leads clinical programming activities on 3-10 concurrent studies depending on scope and resourcing.
• Manages project resources and informs management of delivery and resourcing needs.
• Maintains broad knowledge in clinical programming and data management through literature, training, and conferences.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education may be considered. The Company is committed to compliance with the Americans with Disabilities Act and provides reasonable accommodations as appropriate.