PHARMAFull-time
Senior Clinical DB Designer
BANGALORE (IN)ONSITEPOSTED: 9/5/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Study Build & eCRF Design: Interpret study protocols and design/update eCRFs using third-party or in-house CDMS tools in alignment with CDASH and SDTM standards.
Specifications & Configurations: Create and update Edit Specification Documents and generate specifications for Electronic Data Capture (EDC) build components such as Rights and Roles, System Settings, and Home Page.
Cross-Functional Collaboration: Collaborate closely with Data Team Leads (DTL), Programmers, Validation Teams, Vendors, Statisticians, and Client Representatives. Attend and lead key design meetings including Online Screen Reviews and Internal Design Review Meetings.
Database Administration & LLRR Data: Design databases for collecting LLRR data (e.g., within InForm EDC) and complete administrative setup forms such as Study Authorization and Trial Capacity Requests.
Risk & Financial Management: Identify and communicate project risks or potential timeline delays to DTLs. Monitor project Quality Improvement Plans (QIP) and identify out-of-scope activities from a programming shared services perspective.
Process Improvement: Continuously identify areas for workflow optimization and actively contribute to process improvement initiatives.
Technical & Domain Standards
Strong expertise in CDMS/EDC platforms (e.g., Oracle InForm, Medidata Rave).
Full compliance with CDISC standards, specifically CDASH and SDTM guidelines.
Proficient in generating Edit Checks specifications and database architecture configurations for Phase I-IV clinical trials.
Leadership & Impact
Manage multiple study design projects concurrently across different EDC platforms.
Ensure regulatory compliance, adherence to Standard Operating Procedures (SOPs), and high quality in database builds.
REQUIRED VERIFIED SKILLS
Clinical Database Design
EDC
eCRF Design
CDISC
CDASH
SDTM
InForm
Edit Specifications
Clinical Data Management
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Salaries for Senior Clinical Database Designers with 7+ years of experience in India are competitive within the CRO/Life Sciences industry. Total compensation includes base salary, annual performance bonuses, health benefits, and continuous professional development opportunities.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
EXPECTED CAREER ROADMAP
This role offers a clear progression path toward Lead Clinical Database Designer, Principal DB Designer, Clinical Data Architecture Manager, or Technical Delivery Lead within IQVIA's global clinical data management organization.
APPLICATION ADVISORY
Highlight core hands-on experience with EDC platforms (especially Oracle InForm or Medidata Rave) and strong alignment with CDASH/SDTM standards in your resume. Demonstrate your ability to lead design review meetings and manage out-of-scope deliverables effectively.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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