19 ott - Varese
Icon Clinical
OverviewIn this role you lead the Clinical Trial Liaison (CTL) teams across multi-CTL studies, ensuring high-quality investigator and site support while driving staff development.
You will translate complex science for project teams, build trusted site relationships, and tackle barriers to recruitment and data quality.
The position blends hands-on trial support with people leadership in a global, matrixed environment.
You will shape site engagement strategies and contribute to tools and materials to improve study conduct and performance.
This is a pivotal, impact-focused role within ICON's mission to accelerate patient access to new medicines.
Retribuzione / Benefitscompetitive base salary
performance related incentives
health and wellbeing programmes
retirement and pension plans
life assurance and disability coverage
employee assistance programmes and development opportunities
ResponsabilitàLead CTL activities on multi-CTL studies, coordinating workstreams and ensuring quality and timelines
Manage, mentor, train and coach CTL team members for career development
Translate scientific concepts and protocol details for project teams, investigators and site staff
Create educational materials to communicate trial science and ensure site understanding
Build and maintain relationships with investigators and site personnel to support study conduct
Identify scientific and operational barriers to recruitment, retention and data quality and address them
Identify and optimize pre-screening strategies based on site feedback and patient pathways
Provide detailed, timely reports on investigator/site interactions and insights for project teams
Contribute to tools, materials and strategies supporting site engagement and performance
Participate in business development and represent the CTL function as needed
Requisiti fondamentaliDoctoral-degree level qualification such as PhD, MD or PharmD in a relevant discipline
Substantial experience in clinical research, medical affairs or field-based roles involving investigators and trial sites
Strong understanding of clinical trial design, GCP and site operations
Ability to interpret complex medical information and explain protocol concepts clearly
Proven relationship-building credibility with clinicians, investigators and site teams
Demonstrated leadership and people-management capability including coaching and mentoring
Excellent communication, presentation, influencing and problem-solving skills
Ability to manage competing priorities in a global, matrixed environment
relationship-building
communication
presentation
clinical trial design
Good Clinical Practice (GCP)
site operations
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