Clinical Research Associate

🔥 16 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements. • Conduct on-site visits across the South West UK region, supporting study sites and identifying solutions to operational challenges. • Partner with cross-functional teams to ensure accurate, timely collection and reporting of study data. • Build and maintain strong working relationships with investigators, site staff, and other key stakeholders. • Provide guidance and support to site personnel, helping to ensure the successful delivery of clinical trials.

🎯 Requirements

• A degree in Life Sciences, Nursing, Medicine, or a related discipline. • Previous UK experience as a Clinical Research Associate within oncology studies. • Strong understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP). • Excellent organisational skills, with the ability to manage multiple sites and priorities effectively. • Proven experience in site management, monitoring activities, and ensuring high-quality study delivery. • Strong communication and relationship-building skills. • Willingness and ability to travel to sites across the UK, with a valid driving licence. • 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