Principal Clinical Programmer (Rave/Veeva)

0-2 years
Not Disclosed
10 March 31, 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

 


Principal Clinical Programmer (Rave/Veeva)

Location: India-Asia Pacific - IND-Home-Based
Job ID: 25002054

About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating customer success. We leverage clinical, medical affairs, and commercial insights to bring innovative therapies to market faster.

Job Overview

As a Principal Clinical Programmer (Rave/Veeva), you will be responsible for application administration, technical support, and programming activities for clinical trials. You will lead programming projects, provide technical expertise, and ensure compliance with industry standards and regulatory requirements.

Key Responsibilities

  • Provide technical expertise in clinical programming applications such as Medidata Rave, Veeva EDC, Oracle OC/RDC, and SAS.

  • Develop, validate, and maintain software solutions to support clinical trial data processing.

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

  • Perform system integrations, application updates, and user acceptance testing (UAT).

  • Act as the lead clinical programmer, managing multiple studies and mentoring junior programmers.

  • Participate in project meetings, sponsor audits, bid defenses, and cross-functional discussions.

  • Manage project budgets, timelines, and scope, ensuring high-quality deliverables.

  • Oversee vendor management, ensuring service-level agreements (SLAs) are met.

  • Ensure regulatory compliance by maintaining up-to-date documentation, SOPs, and work instructions.

  • Lead Quick Start Camps (QSCs) and provide training, guidance, and mentorship to programming teams.

Qualifications & Skills

  • Bachelor’s degree (Master’s preferred) in Computer Science, Life Sciences, or a related field.

  • Extensive experience with Medidata Rave OR Veeva EDC for end-to-end clinical programming.

  • Proficiency in PL/SQL, SAS, C#, or VB is preferred.

  • Strong experience in clinical trial programming, system integrations, and data management.

  • Excellent communication, leadership, and problem-solving skills.

  • Ability to manage multiple projects in a fast-paced environment.

  • Experience working in a matrix-structured organization is preferred.

  • Ability to travel up to 25% as required.

Why Join Syneos Health?

  • Work on 94% of FDA-approved drugs in the past five years.

  • Gain global exposure in clinical research.

  • Career growth opportunities with mentorship and professional development.

  • Inclusive and collaborative work culture focused on innovation.