Clinical Data Coordinator

🔥 0 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Data Coordinator

👻 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.

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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

• Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures • Review clinical and third-party data based on edit specifications and data review plans • Issue clear, accurate, and concise queries to investigational sites • Communicate effectively with peers, clinical data scientist and functional management • Perform project activities such as filing and archiving study documentation and dispatching queries to investigator sites for resolution • Ensure study timelines are met

🎯 Requirements

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare • Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry • Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar) • Strong attention to detail and the ability to work effectively in a fast-paced environment • Excellent communication skills and the ability to collaborate with cross-functional teams • Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus • 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