Clinical Trial Associate

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. • Lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement. • Manage and coordinate clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines. • Collaborate with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies. • Oversee site management and monitoring to ensure data integrity and compliance with study protocols. • Provide guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards. • Track and report on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements • Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills • Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders • Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.

🏖️ 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