Senior Clinical Trial Associate

Job not on LinkedIn

🔥 4 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

👻 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

• Support the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines • Coordinate study team meetings, manage meeting minutes and action items • Work effectively with external vendors • Grant and maintain system access • Support study operations activities across multiple stakeholders • Plan weekly team meetings, take minutes, update slides and action logs • Assist in the preparation and review of regulatory documents • Assist with vendor access requests and ancillary supplies, along with vendor management tasks such as UATs • 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 • Provide back-up support to the project manager

🎯 Requirements

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research • 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 • Strong experience with systems, like Veeva Vault, Excel and Vendor portals • Eager to explore and embrace new technologies, systems, and digital solutions to work more efficiently • Experience working on a regional level and capacity • 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 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