Regulatory Affairs Specialist
Clinical Careers Page
About this role
ICON plc is seeking a Regulatory Affairs Specialist to support clinical trial documentation, regulatory submissions, and compliance activities in the pharmaceutical and biotech industries. The role involves collaborating with cross-functional teams and contributing to regulatory intelligence functions.
Skills
Qualifications
About Clinical Careers Page
iconplc.comICON 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.
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About Clinical Careers Page
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
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
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and employee contacts for Clinical Careers Page.
Salary
$45k – $65k
per year
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