Inductive Quotient Analytics India is inviting applications for the position of Clinical Database Designer in Hyderabad. This opportunity is ideal for professionals with 2–3 years of experience in Clinical Data Management (CDM), EDC Programming, Medidata Rave, or Veeva Vault CDMS who are looking to advance their careers in clinical research and database design.

The company specializes in providing end-to-end biometrics services, Clinical Data Management, Biostatistics, Statistical Programming, Medical Writing, Medical Coding, Real World Evidence (RWE), and AI-driven clinical trial solutions. Candidates with expertise in eCRF development, edit checks, dynamics, derivations, and clinical database validation are encouraged to apply.

Job Overview

Key Responsibilities

As a Clinical Database Designer, you will be responsible for:

• Design and develop Electronic Case Report Forms (eCRFs).
• Build clinical databases using Medidata Rave, Veeva Vault CDMS, and other EDC platforms.
• Configure Dynamics, Edit Checks, Derivations, and Data Validation Rules.
• Perform Lab Module configuration and setup.
• Configure IXRS/IWRS and external vendor integrations.
• Conduct database programming, testing, peer review, and validation.
• Support CDASH implementation and data extraction.
• Collaborate with Clinical Data Managers, Sponsors, and cross-functional study teams.
• Maintain database documentation and audit readiness.
• Ensure compliance with ICH-GCP, 21 CFR Part 11, SOPs, and regulatory standards.
• Manage multiple clinical studies while meeting project timelines.

Required Qualifications

Candidates should possess:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline.
• 2–3 years of experience in Clinical Database Design or EDC Programming.
• Hands-on experience with:
  • Medidata Rave
  • Veeva Vault CDMS
  • Other EDC platforms
• Strong understanding of:
  • eCRF Development
  • Edit Checks
  • Dynamics
  • Derivations
  • Lab Module Configuration
  • Clinical Database Validation
  • Data Extraction
• Knowledge of:
  • Clinical Data Management workflows
  • CDASH Standards
  • ICH-GCP
  • 21 CFR Part 11
  • Regulatory Compliance

Preferred Skills

• Clinical Data Management
• EDC Programming
• Medidata Rave
• Veeva Vault CDMS
• CDISC Standards
• Clinical Trial Database Design
• Validation Documentation
• Problem Solving
• Technical Documentation
• Cross-functional Collaboration

Why Join Inductive Quotient Analytics?

Employees joining Inductive Quotient Analytics can benefit from:

• Opportunity to work on global clinical trials
• Exposure to AI-enabled clinical research technologies
• Career growth in Clinical Data Management
• Collaborative work environment
• Experience with leading EDC platforms
• Exposure to regulatory-compliant database development
• Work with experienced clinical research professionals

How to Apply

Application Link