Clinical Trial Associate

🔥 53 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Clinical Trial Associate

👻 Ghost score 10%

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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 in-depth feasibility assessments for clinical trials, including evaluating site capabilities, resource availability, and potential risks • Collaborate with clinical operations teams, project managers, and other stakeholders to gather and analyze data relevant to trial feasibility • Prepare comprehensive feasibility reports and recommendations to support project planning and decision-making processes • Analyze historical data and site performance metrics to identify trends, opportunities, and challenges impacting trial feasibility • Develop and maintain strong relationships with clinical sites, investigators, and external partners • Stay up-to-date with industry trends, regulatory requirements, and best practices related to clinical trial feasibility and planning • Provide mentorship and guidance to junior feasibility team members • Contribute to continuous improvement efforts within the team

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Extensive experience in clinical trial feasibility assessments, with a deep understanding of clinical research processes and site management • Exceptional analytical skills, with the ability to interpret complex data and provide actionable insights • Strong organizational and project management skills, with experience in handling multiple feasibility projects simultaneously • Excellent communication and interpersonal skills, with the ability to build and maintain effective relationships with stakeholders at all levels • Proficiency in data analysis tools and software relevant to feasibility assessments and clinical research • Willingness to travel as required (approximately 15%) • 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

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