Job Title:
Sr Clinical Programmer (EDC Programming – Rave/Veeva)
Location:
Remote (India)
Job ID:
25101762
Company Overview:
Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. By combining clinical, medical affairs, and commercial insights, the company delivers streamlined solutions in clinical development, placing patients and customers at the center of everything.
Learn more: Syneos Health
Job Summary:
The Sr Clinical Programmer serves as a lead clinical programmer managing multiple projects, timelines, and deliverables in Electronic Data Capture (EDC) systems such as Rave and Veeva. This role designs, validates, and maintains software for data capture, reporting, and database management, while acting as a technical SME for internal and external teams.
Core Responsibilities:
Lead clinical programming activities on 3–10 concurrent studies based on scope and resources.
Design, write, validate, and maintain software using Medidata Rave, Oracle OC/RDC, Oracle Inform, SAS, and other supporting tools.
Develop and maintain all project documentation: specifications, programs, annotated CRFs, database creation, coding configuration, edit checks, imports/exports, listings, and custom reports.
Provide technology support to clinical programming staff, project analysts, and data managers.
Serve as the SME for core business packages and supplemental tools (migration mentor/review, reporting tools, custom functions).
Ensure quality deliverables via senior review of study/program/multi-study outputs.
Monitor workflows, system errors, and performance issues; provide second-tier help desk support as needed.
Participate in system integration, application updates, and user acceptance testing.
Provide leadership, guidance, and training to team members.
Collaborate with clients, peers, and project teams to clarify and finalize specifications.
Attend Quick Start Camps (QSCs) as lead programmer for assigned studies.
Maintain broad knowledge in clinical programming and data management through self-learning, training, and professional development.
Qualifications & Experience:
Bachelor’s degree preferred, or equivalent combination of education and experience.
5+ years of experience in clinical programming and database build activities.
Strong Custom Function Programming experience (minimum 4 years).
Minimum 3 years of migration experience (post-database changes) with impact analysis skills.
Expertise in Medidata Rave and iMedidata: edit/form design, dynamic edits, global libraries, eCRF PDF reports.
Ability to interact effectively with sponsors and internal customers at all levels.
Demonstrated experience managing multiple priorities in a dynamic environment.
Experience in matrix-structured organizations preferred.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and voicemail.
Knowledge of programming languages such as PL/SQL, SAS, C#, or VB preferred.
Willingness to travel as necessary (up to 25%).
Skills & Competencies:
Strong leadership, analytical, and problem-solving skills.
Excellent written and verbal communication.
Ability to prioritize and manage multiple projects simultaneously.
Subject Matter Expertise in EDC systems and clinical data management.
Proactive resource and project management.
Impact & Contribution:
Ensures accurate, high-quality deliverables for clinical studies.
Provides SME guidance, mentoring, and technical leadership.
Supports process improvement, vendor integration, and compliance activities.
Job Category:
Clinical Programming / EDC / Clinical Data Management
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