Senior Clinical Research Associate

🔥 6 minutes ago

🌐 Canada, United States – Remote

🇨🇦 Canada – Remote 🇺🇸 United States – Remote

💵 $108.6k - $135.7k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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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 the progress of clinical studies at investigative sites or remotely • Ensure clinical trials are conducted, recorded, and reported according to the protocol • Ensure compliance with standard operating procedures (SOPs), ICH-GCP, and applicable regulatory requirements • Support clinical research for pharmaceutical, biotechnology, medical device, government, and public health organizations

🎯 Requirements

• Bachelor's degree, or its international equivalent, in a scientific or health-related field, or an equivalent combination of education and clinical research experience • 1+ years of clinical monitoring experience or equivalent combination of education and experience required for the level 2 role • 3+ years of clinical monitoring experience required for a level 3 role • Oncology monitoring experience preferred • Ability to travel 70% • Knowledge of ICH and local regulatory authority regulations regarding drug trials • Legally authorized to work in the United States or Canada • Must not require, now or in the future, sponsorship for employment visa status • Bilingual English/French required

🏖️ Benefits

• Competitive base salary • Performance related incentives • 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 • Supportive policies and wellbeing initiatives • Reasonable accommodations during the recruitment process