Clinical Research Associate I – II

🕒 August 11

🇧🇷 Brazil – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 23%

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

• 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 preparing and reviewing 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 through compliance with ICON procedures, protocols, and regulatory requirements • Oversee and coordinate clinical trials, ensuring regulatory compliance and collecting and analyzing critical data

🎯 Requirements

• University degree in medicine, science, or equivalent • Knowledge of ICH-GCP guidelines • Expertise in reviewing and evaluating medical data • Excellent written and verbal communication in English • Good social skills enabling timely handling of queries • Ability to travel at least 60% of the time internationally and domestically • Valid driver’s license • Legal right to work in Brazil

🏖️ 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