Site Engagement Lead

🔥 16 hours ago

🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

👻 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• 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 • 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 each study and site • Monitor site performance metrics and provide regular updates to study teams on site engagement activities and outcomes • Contribute to clinical research activities, taking responsibility for deliverables and working collaboratively

🎯 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%) • 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