Job ID: 25002704
Location: IND – Remote
Updated: August 22, 2025
Syneos Health® is a global, fully integrated biopharmaceutical solutions provider. With 29,000 employees across 110 countries, we deliver clinical, medical affairs, and commercial services designed to accelerate the development and commercialization of therapies.
94% of all novel FDA-approved drugs (past 5 years)
95% of EMA-authorized products
200+ studies conducted across 73,000 sites and 675,000+ patients
Motto: WORK HERE MATTERS EVERYWHERE
🚀 Career Growth & Progression
🌍 Diverse, inclusive, and authentic workplace culture
🧑🏫 Supportive line management and technical mentoring
🛠️ Cutting-edge tools and cross-functional collaboration
🧘 Total Self Culture – Encouraging authenticity and well-being
Provide application administration and technical expertise on clinical tools including:
Medidata Rave, Oracle OC/RDC, Oracle Inform, SAS
Supporting tools (e.g., reporting, migration, custom functions)
Design, develop, validate, and maintain software using standard development procedures
Serve as lead clinical programmer on multiple concurrent studies (5–20 depending on scope)
Generate and maintain specifications, annotated CRFs, edit checks, import/export setups, listings, and custom reports
Conduct system integration, UAT, application upgrades, and proactive performance monitoring
Actively participate in project teams, client discussions, QSCs, bid defenses, and sponsor audits
Supervise and mentor junior programmers; manage performance appraisals and career development
Oversee application vendors and monitor service level agreements (SLAs)
Perform senior-level review of multi-study core programming deliverables
Manage study budgets, project progress, scope tracking, and change orders
Contribute to SOP/work instruction updates and ensure alignment with organizational standards
Resolve programming issues and prioritize deliverables with internal teams and sponsors
Bachelor’s degree required (Master’s preferred) in a relevant field
Equivalent education and experience will be considered
8+ years of end-to-end clinical programming experience in Medidata Rave or Veeva EDC
Strong hands-on experience with:
EDC Study Build
eCRF development
Edit check programming
Migrations & Post-Production Changes (PPC)
Custom Functions (especially for Rave)
Knowledge of programming languages like PL/SQL, SAS, C#, or VB preferred
Familiarity with Microsoft Office Suite (Word, Excel, PowerPoint)
Prior leadership or lead programmer experience is essential
Must have strong problem-solving, multi-tasking, and communication skills
Prior experience in a matrix-structured environment is preferred
Willingness to travel up to 25%
Tasks and responsibilities may be adjusted based on project needs
Equivalent qualifications may substitute those listed
This job posting does not constitute an employment contract
Syneos Health is committed to:
Equal Opportunity Employment (EU Equality Directive)
ADA Compliance (reasonable accommodations available)
🔹 Not ready yet? Join the Talent Network
At Syneos Health, we value diverse perspectives, transferrable skills, and authenticity. Even if your experience doesn’t align perfectly with every requirement, we encourage you to apply and explore how you can make an impact with us.
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