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Principal Clinical Programmer (Rave/Veeva)

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 April 7, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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: Principal Clinical Programmer (Rave + Custom Function/Veeva)


Company: Syneos Health®

Location: India (Home-Based)

Department: Clinical Programming

Updated Date: Not specified (based on job content recency: 2025)


About Syneos Health:

Syneos Health® is a leading, fully integrated biopharmaceutical solutions provider with a global workforce of 29,000 across 110 countries. With a mission to accelerate therapies and change lives, the company integrates clinical, medical, and commercial insights into outcome-driven strategies. Their inclusive Total Self culture fosters authenticity, collaboration, and innovation.


Why Join:

  • Strong career development and progression framework

  • Diverse, inclusive, and supportive workplace culture

  • Industry-leading exposure to major global clinical trials

  • Technical training, peer recognition, and total rewards programs


Job Responsibilities:

  • Serve as SME for core business packages like Medidata Rave, Oracle OC/RDC, Inform, SAS, and Veeva

  • Design, validate, and maintain software for database setup, edit checks, CRFs, imports/exports, and reporting tools

  • Monitor and troubleshoot system issues, workflows, and programming deliverables

  • Lead system integration, application upgrades, and user acceptance testing

  • Coordinate development activities across multiple clinical projects

  • Support project planning and execution, ensuring quality, timelines, and budget alignment

  • Attend client meetings, sponsor audits, and bid defenses

  • Lead or oversee 5–20 concurrent studies; supervise associated programming teams

  • Mentor team members, assign project work, and review performance

  • Manage resources, vendor coordination, and monitor service level agreements (SLAs)

  • Ensure compliance with company SOPs, WIs, and regulatory guidelines

  • Contribute to SOP/process updates and professional knowledge development


Qualifications:

  • Bachelor’s degree required (Master’s preferred); relevant education/experience accepted in lieu

  • Proven end-to-end clinical programming experience in Medidata Rave or Veeva EDC

  • Strong interpersonal and client-handling skills

  • Ability to manage multiple dynamic priorities in a matrix environment

  • Proficient in MS Office Suite; knowledge of PL/SQL, SAS, C#, or VB preferred

  • Travel readiness (up to 25%)


Additional Information:

  • Responsibilities may evolve at the company’s discretion

  • Equivalent education/experience will be considered

  • Fully compliant with ADA and applicable global employment regulations