PHARMAFull-time
Principal Clinical DB Designer
BANGALORE (IN)ONSITEPOSTED: 9/5/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Team & Delivery Management: Oversee a team of clinical database design professionals responsible for the study build and delivery of multiple clinical studies across various EDC and CDMS platforms. Plan, assign, and direct work across project portfolios.
Global Subject Matter Expertise (SME): Serve as a Global SME and global librarian. Support and perform CAPA (Corrective and Preventive Action) investigations, issue management, and escalations. Provide SME guidance to IT teams for software application maintenance and adoption.
Financial & Scope Management: Perform project financial checks and reviews, track budgets and scope assumptions, and identify out-of-scope work to provide revised cost documentation.
Technical Guidance & Review: Provide expert review and guidance on Data Management deliverables including CRF/eCRF creation, database design and setup, validation definitions, and Data Management Plans (DMP) for internal and external customers.
Resource & Process Optimization: Define and prioritize resource requirements, peer-review portfolio tasks, and lead the development and implementation of new technology and clinical trial processes.
Mentorship & Talent Development: Mentor staff to enhance DM programming skills, system knowledge, and drug development expertise. Ensure team compliance with SOPs and address training needs.
Business Development & Client Relations: Act as a primary client contact for database design teams, participate in proposal defenses, contribute design/programming input into proposals, and lead strategic planning discussions with customers.
Technical & Domain Standards
Mastery of EDC/CDMS platform architecture, global library management, and standards enforcement (CDISC, CDASH, SDTM).
Deep understanding of CAPA processes, validation protocols, and regulatory compliance guidelines.
Comprehensive grasp of project financial metrics including burn rates, scope changes, and out-of-scope (OOS) documentation.
Leadership & Impact
Drive global standards, process efficiencies, and technology adoption across multi-center clinical trials.
Manage cross-functional stakeholder relationships, client engagement, and portfolio-level quality control.
REQUIRED VERIFIED SKILLS
Clinical Database Design
EDC
eCRF Design
Global Library Management
CAPA
CDISC
CDASH
SDTM
Data Management Plan (DMP)
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Compensation for a Principal Clinical DB Designer with 10+ years of core technical experience is aligned with senior technology leadership tiers in India's CRO sector. Packages feature high base compensation, performance bonuses, global equity options, and comprehensive health benefits.
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 principal-level leadership role opens direct career paths toward Manager/Director of Clinical Database Architecture, Global Head of Standards, or Director of Data Management Operations within IQVIA or major CRO and biotech organizations.
APPLICATION ADVISORY
Ensure your resume clearly highlights your experience with global library administration, CAPA management, and team leadership across multiple EDC platforms. Emphasize your participation in proposal defenses and financial management of out-of-scope activities.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.