Study Delivery Specialist – Unblinded

Job not on LinkedIn

🔥 9 minutes ago

🇵🇱 Poland – 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

• Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues • Assist in preparing and reviewing regulatory documents, ensuring site activities comply with GCP and applicable regulations • Collaborate with cross-functional teams to facilitate communication and support for trial sites throughout the study lifecycle • Track site performance metrics, analyze data, and provide reports to enhance site management efficiency • Participate in training initiatives and mentor junior staff to support their development in clinical trial management • Contribute to clinical research activities and take responsibility for deliverables

🎯 Requirements

• Master degree in Pharmacy (mandatory) • Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines • Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines • Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards • Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams • 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