Regulatory Affairs Senior Specialist

Clinical Careers Page(2 months ago)

RemoteFull TimeSenior$128,565 - $173,210 (estimated)Regulatory Affairs

About this role

A Regulatory Affairs Senior Specialist at ICON is a senior regulatory professional supporting clinical development within a global healthcare intelligence and clinical research organization. The role is homebased in Estonia and contributes regulatory expertise to pharmaceutical, biotech, and biologics projects while working with cross-functional teams.

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Required Skills

Regulatory Submissions
Label Review
Translation
Regulatory Intelligence
Readability Testing
IMPD Review
Clinical Documentation
Detail Orientation
Communication
Collaboration

Qualifications

Bachelor's Degree in Scientific or Healthcare Field
Advanced Degree Preferred

About Clinical Careers Page

iconplc.com

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.

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