Database Management Specialist (Rave)

IQVIA; Bengaluru; On-site; INR 1,500,000 - 2,800,000; Full time

Job summary

IQVIA is seeking an experienced Medidata Rave Programmer to design, build and validate CRFs and CFs across studies, ensuring data standards and quality. The candidate will contribute to compliant data delivery and support lifecycle management in a global environment.

The role requires 5+ years in Medidata Rave Architect with strong CRF, CF and edit check expertise, plus knowledge of GCP/ICH and regulatory requirements.

Qualifications

• 5+ years of hands-on experience in Medidata Rave Architect.
• CRF Design & Build, Edit Check Development and CF Development expertise.
• Rave migration, study build and validation experience.
• Experience with Medidata Rave eCRF lifecycle management.
• Understanding of clinical trial data collection processes.
• Knowledge of GCP, ICH and regulatory compliance requirements.
• Strong analytical, troubleshooting and communication skills.

Responsibilities

• Design and develop CRFs in Medidata Rave Architect.
• Develop, test, and maintain complex CFs and Edit Checks.
• Review CRF and Edit Check specifications for completeness and accuracy.
• Perform unit testing, UAT support, and validation activities.
• Conduct peer reviews of CRFs, Edit Checks, and CFs.
• Migrate study builds, edit checks, and CFs across environments.
• Support Rave library management and standards implementation.
• Assess impact of Rave upgrades and perform regression testing.
• Collaborate with Clinical Data Management, Programming, and Study Teams.
• Maintain development documentation and ensure SOP/regulatory compliance.

Skills

Medidata Rave Architect

CRF Design & Build

Edit Check Development

Custom Function Development

Rave Migration Activities

Study Build and Validation

Regulatory Compliance (GCP/ICH)

Analytical & Troubleshooting

Communication Skills

Education

Bachelor’s or Master’s degree in Computer Science/ Life Sciences/ Statistics/ Information Systems

Job description

Job Summary

We are seeking an experienced Medidata Rave Programmer with 5+ years of hands‑on experience in Medidata Rave Architect , including CRF design, Edit Check development, and Custom Function (CF) programming. The candidate will be responsible for building, validating, and maintaining Rave studies while ensuring compliance with clinical data standards and quality requirements.

Key Responsibilities

• Design and develop CRFs in Medidata Rave Architect.
• Develop, test, and maintain complex Custom Functions (CFs) and Edit Checks.
• Review CRF and Edit Check specifications for completeness and accuracy.
• Perform unit testing, UAT support, and validation activities.
• Conduct peer reviews of CRFs, Edit Checks, and Custom Functions.
• Migrate study builds, edit checks, and custom functions across environments.
• Support Rave library management and standards implementation.
• Assess impact of Rave upgrades and perform regression testing.
• Collaborate with Clinical Data Management, Programming, and Study Teams.
• Maintain development documentation and ensure compliance with SOPs and regulatory requirements.

Required Skills

• 5+ years of experience in Medidata Rave Architect.
• Strong expertise in:
  • CRF Design & Build
  • Edit Check Development
  • Custom Function (CF) Development
  • Rave Migration Activities
  • Study Build and Validation
• Experience with Medidata Rave eCRF lifecycle management.
• Understanding of clinical trial data collection processes.
• Knowledge of GCP, ICH, and regulatory compliance requirements.
• Strong analytical, troubleshooting, and communication skills.

Preferred Skills

• Experience with Rave Library Management.
• Exposure to Lab Administration module in Rave.
• Knowledge of CDISC standards (SDTM).
• Experience supporting global clinical studies.
• Understanding of metadata-driven clinical data standards. Educational Qualification

Bachelor’s or master’s degree in computer science, Life Sciences, Statistics, Information Systems, or related field

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.