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© All Rights Reserved. ApplyBlast.com
ICON plc
A Senior Pharmacovigilance Associate at ICON leads the collection, evaluation, and processing of adverse event reports to ensure timely regulatory compliance and safety monitoring. The role involves conducting data analysis to identify safety signals, preparing periodic safety update reports, and collaborating with clinical teams to assess adverse events. Additionally, the position requires overseeing database integrity, engaging in regulatory audits, and mentoring junior team members on pharmacovigilance processes.
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.
31% below the average for this role
