Senior CRA

🕒 September 30

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 14%

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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

• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards • Conduct site visits to assess site performance, resolve issues, and provide support for 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 to facilitate smooth trial operations • Oversee and manage clinical trial activities to ensure protocol, regulatory, and industry-standard compliance • Ensure data integrity, participant safety, and compliance throughout the study lifecycle

🎯 Requirements

• Advanced degree in a relevant field such as life sciences, nursing, or medicine • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment • Ability to travel at least 60% of the time (international and domestic - fly and drive) • Valid driver’s license • Legal right to work in Poland

🏖️ 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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