Instagram
youtube
Facebook

Sr Clinical Programmer (Edc Programming-Rave/Veeva)

5+ years
Not Disclosed
10 Sept. 23, 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

Sr Clinical Programmer (EDC Programming – Rave/Veeva)

Location: Hyderabad, India
Job ID: 25101762
Updated: September 11, 2025
Company: Syneos Health®


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions company dedicated to accelerating customer success.

  • 29,000 employees across 110 countries

  • Partnered on 94% of FDA-approved novel drugs in the past 5 years

  • Supported 95% of EMA-authorized products

  • Conducted 200+ studies across 73,000 sites and 675,000+ patients

Why Work Here

  • Career development and progression opportunities

  • Technical and therapeutic training

  • Supportive line management

  • Peer recognition and rewards program

  • Inclusive Total Self culture where authenticity and diversity are celebrated


Job Summary

As a Sr Clinical Programmer, you will:

  • Serve as lead Clinical Programmer for assigned projects

  • Manage and support project deliverables and timelines

  • Design, write, validate, and maintain software to meet study specifications

  • Provide technical SME support for EDC tools, reporting, and processing

  • Support integrations, implementations, and vendor management


Core Responsibilities

  • Develop, validate, and maintain clinical software using:

    • Medidata Rave, Oracle OC/RDC, Oracle Inform, SAS, and supporting tools

  • Generate documentation: specifications, annotated CRFs, edit checks, imports/exports, listings, custom reports

  • Lead project development activities and provide updates on timelines, scope, and budgets

  • Provide technical support to clinical programming, project analysts, and data management teams

  • Administer applications and act as SME for Rave, Inform, RDC, SAS, and related tools

  • Ensure high-quality deliverables with senior-level review and audit readiness

  • Review budgets, track scope vs. actual work, and manage change orders

  • Monitor applications for system errors, performance issues, and workflow alerts

  • Perform system integrations, application updates, and UAT activities

  • Train, mentor, and guide other department members

  • Lead clinical programming activities across 3–10 concurrent studies (depending on scope/resources)

  • Participate in departmental meetings, audits, and sponsor reviews


Qualifications

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

  • Experience: 5+ years total, with:

    • Custom Function Programming: Minimum 4 years

    • Database Migration (post-DB changes): 3+ years, including impact analysis

    • Medidata Rave / iMedidata: Edit & form design, edit check programming, dynamic edits, global libraries, PDF reports

  • Technical Skills:

    • Programming: PL/SQL, SAS, C#, or VB (preferred)

    • Microsoft Office Suite proficiency (Word, Excel, PowerPoint)

  • Other Requirements:

    • Strong communication and interpersonal skills

    • Experience managing multiple priorities in a matrix environment

    • Ability to travel up to 25%


Additional Information

  • Job duties may evolve at the company’s discretion

  • Equivalent experience, skills, or education may be considered

  • Syneos Health complies with ADA and EU Equality Directive (reasonable accommodations available)

  • This posting represents an upcoming opportunity, not a live role


Application

👉 Apply Now
Not ready to apply? Join the Talent Network to stay connected.