Job Title:
Sr Clinical Programmer (EDC Programming – Rave/Veeva)
Location:
Hyderabad, India
Job ID:
25101762
Company Overview:
Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by combining clinical, medical affairs, and commercial insights. The company focuses on streamlining clinical development to efficiently deliver therapies and improve patient outcomes.
Learn more: Syneos Health
Job Summary:
The Sr Clinical Programmer serves as the lead for clinical programming projects, managing deliverables and timelines for EDC systems (Rave/Veeva). Responsibilities include designing, writing, validating, and maintaining software to support data capture, processing, reporting, and database management. This role also provides technical SME support for internal and external teams, assists with vendor integration, and ensures compliance with clinical study specifications.
Core Responsibilities:
Lead clinical programming activities across multiple studies (3–10 concurrent studies).
Utilize development tools including Medidata Rave, Oracle OC/RDC, SAS, and other supporting tools.
Design, write, validate, and maintain software to meet project specifications.
Develop and maintain documentation: specifications, programs, validation efforts, annotated CRFs, database creation, coding configuration, edit checks, imports/exports, listings, and custom reports.
Monitor internally and externally hosted applications for performance, workflow alerts, and system errors.
Provide second-tier technical support and training for clinical programming staff, project analysts, and data managers.
Serve as project SME, coordinate and lead development activities, participate in meetings, and provide status updates to project management.
Assist in managing budgets, scope changes, and change orders.
Perform system integration, application updates, and user acceptance testing.
Lead Quick Start Camps (QSCs) for assigned studies.
Maintain knowledge of clinical programming and data management trends through literature, training, and professional development.
Qualifications & Experience:
Bachelor’s degree preferred, or equivalent combination of education and experience.
5+ years of total experience in clinical programming and database build activities.
Minimum 4 years of Custom Function Programming experience.
Minimum 3 years of experience in migration (post-database changes) with ability to perform impact analysis.
Experience with Medidata Rave and iMedidata: edit/form design, dynamic edits, global libraries, eCRF PDF reports.
Ability to manage multiple priorities in a dynamic, matrix-structured environment.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and email/communication tools.
Experience with programming languages such as PL/SQL, SAS, C#, or VB is preferred.
Willingness to travel as necessary (up to 25%).
Skills & Competencies:
Strong leadership, analytical, and problem-solving abilities.
Excellent written and verbal communication skills.
Ability to interact effectively with sponsors, internal customers, and cross-functional teams.
Proactive management of resources and project deliverables.
Expertise in EDC systems, clinical data management, and clinical study programming.
Impact & Contribution:
Ensures high-quality, accurate, and timely deliverables for clinical studies.
Acts as technical SME and mentor for team members.
Supports process improvements, vendor integration, and regulatory compliance.
Job Category:
Clinical Programming / EDC / Clinical Data Management
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