Principal Clinical Data Standards Consultant Job at ICON – Apply Now!
Looking to advance your career in clinical data standards? ICON plc, a global leader in healthcare intelligence and clinical research, is hiring for the role of Principal Clinical Data Standards Consultant in Chennai and Bangalore. Join a company that’s shaping the future of drug development through innovation, data excellence, and global impact. If you’re passionate about CDISC standards, clinical data strategy, and regulatory compliance, this is the opportunity for you.
About ICON:
ICON plc is a world-renowned clinical research organization that provides outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device industries. Headquartered in Dublin, Ireland, ICON operates in 40+ countries and is committed to improving patients’ lives by accelerating the development of effective medical treatments. At ICON, innovation, integrity, and inclusion drive everything we do.
Job Details:
Job Title: Principal Clinical Data Standards Consultant
Locations: Bangalore, and Chennai
Job Reference: JR128621
About the Role
ICON plc is a global provider of clinical research and healthcare intelligence services. We are currently looking for a Principal Clinical Data Standards Consultant to join our growing team in Bengaluru, Bangalore, or Chennai, India. This is a full-time, office-based role that offers an exciting opportunity to lead data standardization initiatives in global clinical trials.
Key Responsibilities:
-
Lead the development and implementation of CDISC, Sponsor, and ICON clinical data standards.
-
Collaborate with global cross-functional teams to define and manage data collection strategies for clinical research.
-
Create, update, and maintain reference documents and training materials covering CDASH, SDTM, ADaM, define-XML, and submission guidelines.
-
Oversee the design and maintenance of data management tools and processes.
-
Stay up to date with FDA, EMA, and industry regulations to ensure compliance.
Candidate Requirements:
-
Bachelor’s degree (or higher) in Life Sciences, or a related field.
-
Strong experience in clinical data management and data standards within the pharmaceutical or biotech industry.
-
Advanced knowledge of CDISC standards, regulatory frameworks, and clinical data terminology.
-
Excellent communication, analytical thinking, and problem-solving skills.
-
Ability to work collaboratively with cross-functional and international teams.
Why Join ICON?
ICON values diversity, innovation, and personal growth. You’ll enjoy:
-
Competitive salary and benefits
-
Health insurance and wellness programs
-
Retirement planning options
-
Generous leave and flexible working policies
-
Access to 24/7 mental health and employee assistance services
-
Country-specific benefits like gym memberships, travel subsidies, and more
Keywords: Clinical Data Standards Consultant, ICON, Bengaluru, Bangalore, Chennai, Healthcare, Clinical Research, CDISC, Pharmaceutical, Biotechnology
