PHARMAFull-time
Principal Clinical Data Standards Consultant
BANGALORE (IN)HYBRIDPOSTED: 8/13/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Provide expert-level functional guidance in clinical data standards, developing internal and sponsor-facing standards content.
Develop, implement, and maintain ICON end-to-end Data Collection standards libraries aligned with CDISC, CDASH, Controlled Terminology, and regulatory guidelines.
Provide internal and external consulting to sponsors regarding CDISC standards compliance, implementation, and governance frameworks.
Lead cross-functional strategy for clinical data collection, participating in governance meetings and developing standards training materials.
Mentor junior team members, lead departmental process improvement initiatives, and resolve complex clinical data standards challenges.
REQUIRED VERIFIED SKILLS
CDISC
CDASH
Clinical Data Standards
Controlled Terminology
Clinical Data Management
Data Governance
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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