Clinical Research Associate II / Senior Clinical Research Associate

🔥 0 minutes ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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, routine monitoring, and close-out visits • Ensure protocol compliance, patient safety, data quality, and regulatory adherence • Build strong relationships with investigative sites and key stakeholders • Identify and proactively resolve site and study issues • Collaborate with cross-functional teams to support successful study delivery • Support inspection readiness and high-quality study execution • Mentor and guide less experienced CRAs at Senior CRA level

🎯 Requirements

• CRA II: Bachelor's degree in a scientific, healthcare, or related field • CRA II: Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry • CRA II: Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices • CRA II: Ability to work independently while collaborating effectively across teams • Senior CRA: Significant clinical monitoring experience across multiple studies and sites • Senior CRA: Advanced knowledge of clinical trial processes, regulations, and site management • Senior CRA: Proven ability to manage priorities and drive study quality independently • Experience mentoring or supporting other CRAs is advantageous • Strong communication and relationship-building skills • Willingness to travel as required • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive compensation and benefits package • 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 • Career development and support network • Dedicated sponsor environments • Diverse opportunities across multiple therapeutic areas