Clinical Site Manager

Job not on LinkedIn

🔥 0 minutes ago

🇵🇱 Poland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 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

• Build and maintain strong relationships with investigators, site staff, and key stakeholders • Lead site engagement initiatives to optimise site performance and study delivery • Conduct site visits, including qualification, initiation, monitoring, and close-out visits • Act as the primary point of contact for study sites throughout the trial lifecycle • Support site identification, selection, and activation activities • Collaborate closely with Clinical Project Managers, study teams, CROs, and vendors • Ensure high-quality data collection, regulatory compliance, and inspection readiness • Support investigator training and study-related meetings • Contribute to study management activities, including vendor oversight, documentation, and trial tracking

🎯 Requirements

• Bachelor's degree in Life Sciences or a related discipline • 5+ years of experience within a Pharmaceutical, Biotechnology, or CRO environment • Strong clinical trial monitoring experience and knowledge of ICH-GCP guidelines • Previous experience in a site-facing role such as CRA, Clinical Trial Manager, Clinical Project Manager, or Site Engagement professional • Excellent communication and stakeholder management skills • Comfortable working in a fast-paced, international environment • Able to travel regularly • Legal right to work in Poland

🏖️ 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