Clinical Research Associate, Sponsor Dedicated

Clinical Careers Page(2 days ago)

FloridaOnsiteFull TimeMedior$60,000 - $80,000Clinical Research

About this role

A Clinical Research Associate II at ICON plays a key role in monitoring clinical trials, ensuring compliance with protocols and regulations, and collaborating with investigators to facilitate study conduct. The role involves data review, documentation, and supporting the advancement of medical treatments in late phase studies.

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Required Skills

clinical Trials
ICH-GCP
Data Review
Monitoring
Regulations
Study Documentation
Patient Safety
Collaboration
Clinical Data
Interpersonal Skills

Qualifications

Bachelor's Degree in a Scientific or Healthcare-related Field

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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