Senior CRA

🕒 May 26

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

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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

• Oversee and manage clinical trial activities according to protocols, regulatory requirements, and industry standards • Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards • Conduct site visits to assess performance, resolve issues, and support successful trial execution • Collaborate with cross-functional teams on timely and accurate data collection and reporting • Provide training and guidance to site staff and other CRAs • Build and maintain relationships with site personnel and stakeholders • Ensure data integrity, participant safety, and compliance throughout the study lifecycle

🎯 Requirements

• Must have 7 years' experience minimum working as a CRA • Must be based in the UK • Advanced degree in a relevant field such as life sciences, nursing, or medicine • Extensive experience as a Clinical Research Associate (7+ years' minimum required) • Must have at least 2 years' experience working on Oncology studies • Proven ability to manage multiple sites and projects simultaneously • Strong organizational and problem-solving skills • Expertise in monitoring practices, data integrity, and site management • Proficiency in relevant clinical trial software and tools • Excellent communication, interpersonal, and stakeholder management skills • Ability to influence and drive compliance within a complex environment • Ability to travel at least 60% of the time, including international and domestic travel by air and car • Must possess a valid driver's license • Must have the 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

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