PHARMAFull-time
CDS / Sr CDC
BANGALORE (IN)ONSITEPOSTED: 8/13/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Serve as a Data Operations Coordinator (DOC) or secondary lead for clinical study protocols with lower operational complexity.
Conduct clinical data review, generate and resolve data clarification queries, and support central laboratory data processing.
Develop, test, and perform quality checks on clinical database setups, entry screens, and validation edit specifications.
Perform clinical data coding and participate in database audit activities under senior CDM guidance.
Maintain compliance with standard operating procedures (SOPs), working instructions, and good clinical practice standards.
REQUIRED VERIFIED SKILLS
Clinical Data Management
Data Cleaning
Data Clarifications
Clinical Coding
Database Testing
Medical Terminology
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
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
RECOMMENDED TRAINING
1/5
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