ICON plc
The Principal Clinical Data Standards Consultant at ICON designs and analyzes clinical trials while interpreting complex medical data to advance innovative treatments. This role involves coordinating consulting and advisory services, resolving issues, and developing team capability. The position focuses on implementing data standards and collaborating with cross-functional teams to define data collection strategies for clinical trials.
ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for ICON plc.
ICON plc didn’t post a salary, so this is our estimate from similar listings.
Associate Director, Clinical Data Standards and Governance
penfield
FSP Principal Biostatistician, Medical Affairs
IQVIA
Senior Manager, Clinical Data Standards
Bristol Myers Squibb
Principal Programmer ( Data Oversight & Standards)
CSL Behring Australia
Associate Principal Statistical Programmer, Submission Data Standards Quality Management (SDS QM)
MSD
Associate Director, Clinical Standards
AstraZeneca