Clinical Research Associate II

🕒 June 26

🏄 California – Remote

🏄 California – Remote

💵 $91.3k - $114.2k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 20%

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.

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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

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively • 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

🎯 Requirements

• Bachelor's degree in a scientific or healthcare-related field • Minimum of 2 years of experience as a Clinical Research Associate • 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 (approximately 60%)

🏖️ 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