Senior Clinical Research Associate

🔥 6 minutes ago

🌵 Arizona, California, +6 more states – Remote

🌵 Arizona – Remote 🏄 California – Remote ⛰️ Colorado – Remote 🦬 Montana – Remote 🎰 Nevada – Remote 🌶️ New Mexico – Remote 🌲 Oregon – Remote ☕ Washington – Remote

💵 $110.5k - $138.2k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 0%

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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

• Work in a sponsor-dedicated model supported by ICON’s global expertise • Support one study in the cardiovascular/electrophysiology medical device space for A-fib • Monitor clinical trial sites and manage site-related risks and issues • Establish and maintain working relationships with site personnel, investigators, and internal teams • Execute communication plans with study teams and sites • Manage multiple priorities and produce rigorous, detailed, and precise reports • Cover up to 65% regional travel

🎯 Requirements

• 3 years of monitoring experience required • A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science • In-depth knowledge of FDA regulations and ICH/GCP guidelines • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely • Ability to tailor communication style to the needs and preferences of different stakeholders • Ability to work independently and manage multiple priorities in a dynamic environment • Well-versed in clinical trial management • Located in the West region in the US near a major airport • Ability to cover up to 65% regional travel • 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