PHARMAFull-time
Principal Clinical Data Standards Consultant
BANGALORE (IN)REMOTEPOSTED: 8/14/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Develop, implement, and maintain ICON end-to-end clinical data collection and analysis standards libraries in alignment with CDISC and regulatory requirements.
Serve as subject matter expert providing internal and sponsor-facing consulting on CDISC compliance, CDASH, SDTM, and Controlled Terminology.
Participate in data standards governance, defining cross-functional data collection strategies and driving best practices across clinical trials.
Lead complex problem-solving initiatives, mentor junior team members, and oversee departmental project teams.
Design and deliver training materials and reference documentation on data standards for internal teams and external sponsors.
REQUIRED VERIFIED SKILLS
Clinical Data Standards
CDISC
CDASH
SDTM
Controlled Terminology
Data Management
Standards Governance
Consulting
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
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.