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Clinical Research Associate 1 at ICON plc - ApplyBlast

Clinical Research Associate 1

ICON plc

4 months ago

Reading, United Kingdom

Hybrid

Full Time

Senior

0 applicants

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About this role

This role is for a UK home-based In Vitro Diagnostics Clinical Research Associate at ICON, transitioning candidates from lab settings to clinical trial operations. The position involves leading the design, planning, coordination, and execution of clinical research studies specifically for in vitro diagnostics products. Key duties include ensuring regulatory compliance with FDA, GCP, and IVD directives, validating product performance claims, and supplying data for critical regulatory submissions.

Responsibilities

Lead design and coordination of clinical research studies for in vitro diagnostics
Ensure studies adhere to protocols, operating procedures, and regulatory guidelines
Validate product performance claims for consistency and efficacy
Supply critical data for regulatory submissions to relevant authorities
Implement SOPs to maintain compliance with FDA and IVD directive requirements

Skills

Qualifications

Bachelor's degree in Medicine

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

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.