Clinical Research Associate – Level 1

🔥 33 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Deliver clinical trial monitoring work to a high standard • Work closely with the team and stakeholders • Ensure studies are conducted according to study protocols, operating procedures, and good clinical practice • Validate product performance claims • Supply data for critical Regulatory submissions • Define the functional and clinical utility of investigation products • Understand and implement federal regulations • Help roll out SOPs to ensure studies adhere to FDA regulations, GCP, IVD directives, and client policy • Contribute to designing, planning, coordinating, and conducting activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics

🎯 Requirements

• University degree in medicine, science, or equivalent • Practical knowledge of in vitro diagnostics and clinical trial processes • Excellent written and verbal communication in English • Good social skills enabling you to deal with queries in a timely manner • Willingness to travel as required from your UK base (occasionally internationally) • Relevant In Vitro Diagnostics experience, ideally from a laboratory background • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways