Central Review Coordinator

🔥 21 hours ago

🇿🇦 South Africa – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 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

• Conduct risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies. • Collaborate with cross-functional teams to develop and implement risk management plans and protocols. • Monitor data quality and integrity throughout the trial process, reporting findings to stakeholders. • Utilize statistical analysis and visualization tools to communicate risk-related insights effectively. • Support the preparation of risk management documentation for regulatory submissions and audits. • Deliver clinical research work to a high standard while working closely with the team and stakeholders.

🎯 Requirements

• Degree in statistics, life sciences, or a related field. • Experience in clinical data analysis or risk management within a clinical research environment. • Strong analytical skills with proficiency in statistical software and risk assessment methodologies. • Attention to detail and a proactive approach to identifying and addressing data risks. • Effective communication skills, with the ability to collaborate across diverse teams and convey complex information clearly. • Employment with ICON is contingent upon having the 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