Site Engagement Lead

ICON plc

. Build and maintain strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff .

Posted 10/14/2026full-timeRemote • CanadaSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research and site management, with a strong focus on stakeholder engagement, regulatory compliance, and performance optimization. Proven ability to communicate effectively and manage multiple tasks in a dynamic environment.

Highest-signal resume keywords

Clinical Research ExperienceSite ManagementKnowledge of ICH-GCP GuidelinesInterpersonal Communication SkillsOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchSite ManagementRegulatory RequirementsPerformance Metrics MonitoringStudy Protocols

Soft Skills

Interpersonal SkillsCommunication SkillsProblem-Solving SkillsOrganizational Skills

Industry Keywords

Clinical TrialsStakeholder EngagementSite Performance OptimizationResearch Staff CollaborationTravel Willingness

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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