Clinical Research Associate

🔥 6 minutes ago

🏈 Ohio, Pennsylvania, +1 more states – Remote

🏈 Ohio – Remote 🔔 Pennsylvania – Remote ⚔️ Virginia – Remote

💵 $91.3k - $114.2k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 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

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials • Ensure protocol compliance, data integrity, and patient safety throughout the trial process • Collaborate with investigators and site staff to facilitate smooth study conduct • Perform data review and resolution of queries to maintain high-quality clinical data • Contribute to the preparation and review of study documentation, including protocols and clinical study reports • Work in a sponsor-dedicated model supported by ICON’s global expertise

🎯 Requirements

• Bachelor's degree in a scientific or healthcare-related field • Minimum of 2 years of experience as a Clinical Research Associate • Oncology monitoring experience required • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines • Strong organizational and communication skills, with attention to detail • Ability to work independently and collaboratively in a fast-paced environment • Willingness to travel as required up to 50% within their region (Northeast) • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and 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