Clinical Research Associate

🔥 15 minutes ago

🌾 Nebraska, Missouri, +1 more states – Remote

🌾 Nebraska – Remote 🏰 Missouri – Remote 🤠 Texas – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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

• Deliver clinical trial monitoring work to a high standard • Coordinate all activities for setting up and monitoring a study • Complete accurate study status reports and maintain study documentation • Run sponsor-generated queries efficiently and take responsibility for study cost efficiency • Participate in the preparation and review of study documentation and feasibility studies for new proposals as required • Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff • Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements

🎯 Requirements

• University degree in medicine, science, or equivalent • Knowledge of ICH-GCP guidelines • Expertise to review and evaluate medical data • Excellent written and verbal communication in English • Good social skills enabling you to deal with queries in a timely manner • Willingness to travel as required (approximately 60%) • Employment contingent upon having the legal right to work in the country where the role is based • Experience monitoring Ophthalmology trials or multi-TA • Relevant clinical trial monitoring experience

🏖️ 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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