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Senior Clinical Programmer (Veeva Cdb)

2-5 years
Not Disclosed
10 Nov. 26, 2025
Job Description
Job Type: Full Time 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

Senior Clinical Programmer (Veeva CDB) – Syneos Health

Location: Hyderabad, India
Job Type: Full-Time
Job ID: 25102615
Updated: November 10, 2025
Category: Clinical Programming / Data Acquisition

Syneos Health is a leading global biopharmaceutical solutions organization supporting clinical development, medical affairs, and commercial execution. With operations across 110 countries and a team of over 29,000 professionals, Syneos Health partners with clients to accelerate clinical studies, streamline data workflows, and improve patient outcomes.

This role places you at the center of our data-driven clinical programming ecosystem, with a strong focus on Veeva CDB (Clinical Database) and advanced data acquisition environments.


Role Overview

The Senior Clinical Programmer (Veeva CDB) supports end-to-end clinical data programming activities, including database development, data acquisition workflows, and technical system administration. You will lead programming efforts across multiple studies, serve as a subject matter expert for Veeva CDB, and collaborate with cross-functional teams to ensure delivery of high-quality clinical datasets and reports.

You will work in a dynamic environment that values innovation, technical excellence, and operational efficiency.


Key Responsibilities

Clinical Programming & Database Development

  • Utilize primary tools such as Veeva CDB, Medidata Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, build, validate, and maintain clinical databases and programs.

  • Develop specifications, CRFs, edit checks, coding configurations, import/export setups, listings, and custom reports.

  • Maintain thorough documentation for all programming tasks in compliance with development standards.

Project Leadership & Cross-Functional Collaboration

  • Lead programming activities across 3–10 concurrent studies, depending on scope and complexity.

  • Participate in project meetings, ensure timely communication of risks, and provide proactive solutions to meet timelines and quality expectations.

  • Support project analysts, data managers, and clinical programming teams with technical troubleshooting and workflow optimization.

Technical Administration & System Support

  • Serve as a functional SME for Veeva CDB, Oracle Inform, Rave, SAS, and related systems.

  • Oversee application integration, system updates, validation activities, and UAT.

  • Monitor systems for workflow alerts, performance issues, and escalated help desk requests.

Quality Assurance & Compliance

  • Provide senior-level review of study deliverables to ensure accuracy and compliance.

  • Participate in sponsor audits and internal quality assessments.

  • Support scope management, prepare inputs for change orders, and ensure completion of contractual updates.

Training, Mentoring & Knowledge Development

  • Mentor junior programmers and cross-functional team members.

  • Stay up to date with clinical data management trends, system advancements, and regulatory expectations.

  • Contribute to departmental learning sessions, Quick Start Camps (QSCs), and technical best practices.


Experience Required

  • Minimum 2 years of hands-on experience with Veeva CDB in a Senior/Principal-level role
    OR

  • 5+ years of experience in Clinical Data Acquisition, EDC programming, Data Imports, DTA/DTS processes, and program writing.

  • Strong experience working with external vendors, data mapping, and data transfer agreements.

  • Experience with PL/SQL, SAS, C#, or VB is preferred.

  • Proven ability to work in matrix teams and manage multiple study deliverables.

  • Prior experience mentoring or leading programming teams is highly desirable.


Qualifications

  • Bachelor’s degree in life sciences, computer science, data management, or related field (or equivalent experience).

  • Expertise in Veeva CDB as an administrator and SME.

  • Strong knowledge of EDC systems, clinical database design, and data acquisition workflows.

  • Excellent written and verbal communication and strong interpersonal skills.

  • Ability to work with global teams and interact with clients at all levels.

  • Proficiency in Microsoft Office Suite.

  • Willingness to travel up to 25%.


Why Join Syneos Health

  • Strong focus on career development, training, and technical upskilling.

  • A supportive culture that promotes authenticity, diversity, and inclusion.

  • Work on cutting-edge technologies and contribute to global clinical programs.

  • Opportunity to impact the delivery of life-changing therapies across the world.


About Syneos Health

Over the last five years, Syneos Health has partnered on:

  • 94 percent of all novel FDA-approved drugs

  • 95 percent of EMA-authorized products

  • 200+ global clinical studies

Syneos Health continues to innovate and support sponsors in accelerating clinical research and enhancing patient outcomes.


Additional Information

This job description outlines primary responsibilities but is not exhaustive. Tasks may change based on operational needs. The company complies with all global employment laws, including ADA accommodations and equal opportunity regulations.