Clinical Research Associate

🔥 0 minutes ago

🏖️ New Jersey, New York, +1 more states – Remote

🏖️ New Jersey – Remote 🗽 New York – Remote 🔔 Pennsylvania – Remote

💵 $75.5k - $94.3k / 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

• Coordinate all activities for setting up and monitoring a clinical 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 procedures, protocols, and regulatory requirements • Deliver clinical trial monitoring work to a high standard across clinical programs

🎯 Requirements

• University degree in medicine, science, or equivalent • Relevant clinical trial monitoring experience • Experience monitoring Ophthalmology trials or multi-TA preferred by the client • Knowledge of ICH-GCP guidelines • Expertise to review and evaluate medical data • Excellent written and verbal communication in English • Good social skills enabling timely handling of queries • Willingness to travel as required, approximately 60% • Legal right to work in the country where the role is based

🏖️ 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