Senior Clinical Trial Associate

Job not on LinkedIn

🔥 18 hours ago

🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

👻 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

• Oversee and support the execution of sponsor-dedicated oncology clinical trials • Lead clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement • Manage and coordinate clinical trial activities according to protocols, regulatory requirements, and project timelines • Collaborate with cross-functional teams to address trial issues and optimize processes • Oversee site management and monitoring to ensure data integrity and protocol compliance • Provide guidance and support to clinical staff and investigators • Track and report trial progress, identify risks, and implement mitigation strategies

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements • Proven ability to manage multiple projects effectively • Strong organizational and problem-solving skills • Excellent communication and interpersonal skills • Detail-oriented with a proactive approach • Oncology experience required • Solide connaissance des BPC (ICH-GCP) et des exigences réglementaires applicables aux essais cliniques • Expérience en soutien à la gestion et au suivi des centres investigateurs • Capacité à travailler de façon autonome tout en collaborant efficacement avec diverses parties prenantes • 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