Senior Study Start Up Associate

🔥 20 minutes ago

🇳🇱 Netherlands – Remote

⏰ Full Time

🟠 Senior

✨ Associate

👻 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

• Work in a sponsor-dedicated model supported by ICON’s global expertise • Support the Study Start Up Team Lead in developing and executing the plan for country and site distribution in the Netherlands • Acquire approval from Health Authorities and via the CTIS application to start up assigned clinical trials • Lead site start-up and activation tasks with technical depth, focusing on quality and continuous improvement • Conduct feasibility assessments and site identification • Negotiate site contracts and perform other critical study start-up activities • Provide expertise to Study Start Up team leads and project teams • Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies • Contribute to developing, finalizing, and reviewing Master and Country Specific Subject Information Sheets/Informed Consent Forms

🎯 Requirements

• A Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline • At least 3 years of experience or understanding of clinical study start-up requirements and activities • Experience in Clinical Trial Submissions for the Netherlands • Fluency in the local language and English • Willingness to travel as required (approximately 5%) • 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