PHARMAFull-time
CDC II/ Sr CDC
CHENNAI (IN)HYBRIDPOSTED: 8/14/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Assist Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and Study Specific Procedures.
Perform clinical and third-party data reconciliation based on edit specifications and data review plans.
Track and communicate study status and task metrics to clinical data scientists, project teams, and functional management.
Investigate and resolve data-related issues by identifying root causes and recommending solutions.
Ensure data management deliverables adhere to high quality standards and regulatory guidelines such as ICH-GCP.
REQUIRED VERIFIED SKILLS
Clinical Data Management
eCRF
Medidata EDC
Oracle RDC
Third-Party Data Reconciliation
Data Validation Specifications
Edit Checks
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
ICON plc is a global provider of outsourced drug development and commercialization services to pharmaceutical, biotechnology, medical device, and government organizations. The company specializes in a broad range of clinical research services, from Phase I-IV studies to consulting and data solutions. ICON helps its clients accelerate the development of drugs and devices through comprehensive scientific and operational expertise.
TEAM SIZE: 41,100+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
RECOMMENDED TRAINING
1/5
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