Site Care Partner

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🕒 April 9

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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

• Foster relationships with clinical trial sites, enhancing site engagement. • Contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. • Build and maintain strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff. • Provide support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct. • Identify opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms. • Collaborate with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site. • Monitor site performance metrics and provide regular updates to study teams on site engagement activities and outcomes.

🎯 Requirements

• Bachelor's degree in life sciences or a related field. • Previous experience in clinical research, site management, or a related field preferred. • Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders. • Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously. • Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials. • Willingness to travel as required (approximately 60%)

🏖️ Benefits

• Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs. • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.