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Sr Clinical Programmer (Edc Programming-Rave/Veeva)

0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Sr Clinical Programmer (EDC Programming – Rave/Veeva)

Company: Syneos Health®
Location: Remote (IND)
Job ID: 25101762
Updated: September 11, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our Clinical Development model places the customer and patient at the center, and we focus on simplifying and streamlining processes to make our organization easier to work with.

Key Highlights:

  • 29,000 employees across 110 countries.

  • Worked with 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products over the past 5 years.

  • Engaged in over 200 studies across 73,000 sites and 675,000+ trial patients.

Culture:

  • Total Self culture – be authentically yourself.

  • Career development, peer recognition, technical and therapeutic training, and total rewards.

  • Inclusive and diverse workplace fostering belonging.


Job Summary

The Sr Clinical Programmer serves as the lead for clinical programming projects, managing deliverables and timelines. The role involves designing, writing, validating, and maintaining software for Electronic Data Capture (EDC), reporting, and data processing tools. This role acts as the first-level Subject Matter Expert (SME), providing guidance to production-line programming and data management staff, monitoring applications, and assisting with external vendor integrations.


Core Responsibilities

  • Develop, validate, and maintain software using Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and other tools.

  • Generate and maintain documentation: specifications, programs, validations, annotated CRFs, database creation, coding, edit-checks, import/export setup, listings, and custom reports.

  • Lead and coordinate clinical programming activities across projects; participate in meetings and provide constructive feedback.

  • Support clinical programming staff, Project Analysts, and Data Managers with technical guidance and troubleshooting.

  • Administer and provide SME support for core business packages and supplemental tools.

  • Ensure high-quality deliverables via senior review and participation in sponsor audits.

  • Monitor applications for workflow alerts, system errors, and performance issues; provide help desk support as needed.

  • Perform system integration, application updates, and user acceptance testing.

  • Provide leadership, training, and guidance to department members.

  • Lead programming activities on 3–10 concurrent studies based on scope and resourcing.

  • Manage project resources, proactively alerting management about delivery and resourcing needs.

  • Maintain broad knowledge in clinical programming and data management through literature, training, and professional development.


Qualifications

  • Bachelor’s degree preferred, or equivalent combination of education and experience.

  • 5+ years of experience in clinical programming and database build activities.

  • 4+ years of experience in Custom Function Programming.

  • Minimum 3 years of experience in migration (post-DB changes), including impact analysis.

  • Hands-on experience with Medidata Rave and iMedidata, including edit programming, dynamic edits, global libraries, and eCRF PDF report generation.

  • Ability to interact effectively with sponsors and internal customers.

  • Excellent communication and interpersonal skills.

  • Experience managing multiple priorities in a dynamic, matrix-structured environment.

  • Proficient in Microsoft Office Suite.

  • Knowledge of PL/SQL, SAS, C#, or VB preferred.

  • Willingness to travel up to 25%.


Additional Information

  • Tasks and responsibilities are not exhaustive; the company may assign additional duties as needed.

  • Equivalent experience, skills, and education will be considered.

  • Compliance with local legislation and Americans with Disabilities Act (ADA) is ensured.


Summary

The Sr Clinical Programmer leads clinical programming projects, designs and validates software, supports EDC and reporting tools, and acts as a technical SME. The role involves managing multiple studies, mentoring staff, ensuring high-quality deliverables, and supporting system integrations and application maintenance.