Clinical Trial Associate – Study Start-Up Support

🔥 10 minutes ago

🌲 North Carolina, Missouri, +2 more states – Remote

🌲 North Carolina – Remote 🏰 Missouri – Remote 🔔 Pennsylvania – Remote 🤠 Texas – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 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

• Ensure vendor spreadsheets are completed correctly and processed according to study team guidelines • Submit vendor spreadsheets to the vendor or global team • Attend weekly Study Team meetings and report on vendor spreadsheets • Participate in vendor management activities • Work in a sponsor-dedicated model supported by ICON’s global expertise

🎯 Requirements

• Bachelor's degree or relevant clinical trial experience • Industry experience in clinical trial support required (CRO/Pharma) with a focus on vendor support during Start-Up • Experience with vendor management • Strong verbal & written communication skills • Strong organizational skills • Previous administrative experience • Proven organizational and administrative skills • Computer proficiency • Excellent organization and time management skills • Excellent attention to detail and ability to multi-task in a high-volume environment with shifting priorities • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities • Working knowledge of the Clinical Study Process • Understanding of working procedures relating to study Start-up • Understanding of ICH/GCP guidelines • Ability to develop advanced computer skills to increase efficiency in day-to-day tasks • Good interpersonal skills and ability to work in an international team environment • Willingness and ability to train others on study administration procedures • 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