Senior Clinical Trial Associate

🔥 1 minute ago

🇫🇷 France – Remote

⏰ Full Time

🟠 Senior

✨ Clinical Trial Associate

👻 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.

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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

• Take ownership of clinical trial management deliverables and apply expertise to complex challenges • Provide administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records • Assist in preparing and submitting regulatory documents and ensure compliance with study protocols and regulatory requirements • Collaborate with cross-functional teams to support trial operations and resolve study issues • Monitor and track trial progress, including managing site communications and ensuring timely delivery of study materials • Build and maintain relationships with site staff and stakeholders to facilitate smooth trial operations and project success

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements • Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively • Proficiency in clinical trial management systems and relevant software • Keen eye for detail in documentation and data management • Excellent communication, interpersonal, and problem-solving skills • Ability to work collaboratively with diverse teams and stakeholders • Willingness to travel as required (approximately 10%) • Legal right to work in France

🏖️ 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