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Principal Clinical Programmer (Veeva /Rave)

8-10 years
Not Disclosed
10 Dec. 10, 2025
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Principal Clinical Programmer (Veeva / Rave) – Hybrid | Hyderabad, India

Location: Hyderabad, India (Hybrid)
Job ID: 25103365
Status: Position Closed / No Longer Active

About the Role

Syneos Health is seeking an experienced Principal Clinical Programmer with strong expertise in Veeva and Medidata Rave to support global clinical development programs. This senior-level role contributes directly to the design, build, validation, and maintenance of Electronic Data Capture (EDC) systems while collaborating closely with clinical, data management, and technical teams.

Although this job posting is no longer active, the following information outlines the role’s responsibilities and qualifications for future opportunities within the organization.


Key Responsibilities

  • Lead end-to-end clinical programming activities across multiple studies within global clinical development programs.

  • Configure, develop, and validate EDC systems (Veeva / Medidata Rave) following study requirements and regulatory guidelines.

  • Provide technical oversight on database design, edit checks, derivations, manual review plans, and system integrations.

  • Collaborate with cross-functional teams including clinical data management, biostatistics, and clinical operations.

  • Identify process optimization opportunities and contribute to global programming standards.

  • Ensure documentation completeness and inspection readiness in alignment with organizational SOPs, Work Instructions, and regulatory expectations.

  • Mentor junior programmers and provide subject-matter expertise for complex programming tasks.

  • Participate in sponsor discussions, kick-off meetings, and technical reviews as required.


Required Experience

  • Minimum 8–10 years of clinical programming experience, with strong hands-on expertise in Veeva EDC and Medidata Rave.

  • Proven experience leading EDC development across multiple global clinical studies.

  • Strong understanding of CDISC standards, clinical data flow, and regulatory requirements.

  • Experience in a Functional Service Provider (FSP) or large CRO environment preferred.

  • Advanced technical background including database design, edit check programming, and system validation.


Education & Skills

  • Bachelor’s degree in Computer Science, Life Sciences, Statistics, or a related discipline (or equivalent experience).

  • Strong analytical, documentation, and problem-solving skills.

  • Excellent communication skills with the ability to collaborate across global teams.

  • Proficiency in English (reading, writing, and speaking).

  • Ability to manage complex projects, multiple deadlines, and dynamic timelines.


Why Syneos Health

  • A global biopharmaceutical solutions organization with over 29,000 employees across 110 countries.

  • Strong focus on talent development, progression opportunities, and technical training.

  • Supportive leadership, a culture of collaboration, and a commitment to employee well-being through the Total Self culture.

  • Direct involvement in developing 94% of all FDA-approved novel drugs and 95% of EMA-authorized products over the past five years.


Additional Information

Responsibilities listed are not exhaustive. Syneos Health may modify or assign additional tasks at its discretion. Equivalent skills and experience may be considered. The company complies with global employment regulations, including ADA and EU Equality guidelines.