Site Engagement Liaison Manager
Employer · 270 ICR Hungary - HUN
R&D manager
Other health professional
Health services managerFull-timeBudapest
As a Manager, Site Engagement Liaison at ICON, you will lead efforts to build and maintain strong relationships with clinical trial sites, ensuring effective communication and collaboration throughout the study lifecycle in a sponsor-dedicated model.
Tasks
- Build and maintain strong relationships with investigators, site staff, and key stakeholders to support successful study delivery.
- Act as the primary liaison between sites, CRO partners, and internal study teams, ensuring effective communication and collaboration.
- Evaluate site capabilities and performance to support site identification, feasibility, and selection activities.
- Oversee site-level study start-up, activation, conduct, and close-out activities.
- Support site contracting and activation activities in partnership with internal teams and external vendors.
- Monitor site performance, recruitment, enrollment, quality, and compliance metrics.
- Drive site engagement strategies and develop action plans to improve site performance, recruitment, and retention.
- Provide oversight of CRO-delivered site management activities and ensure compliance with ICH-GCP.
- Collaborate closely with Clinical Operations, Study Management, Medical Affairs, Regulatory Affairs, and other cross-functional stakeholders.
- Utilize site and study performance data to identify trends and support decision-making.
Conditions & benefits
Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathways
Requirements
- Degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related scientific discipline.
- 8+ years of clinical research experience within a CRO, pharmaceutical, biotechnology, or healthcare environment.
- Strong understanding of clinical trial conduct, global drug development, ICH-GCP, and applicable regulatory requirements.
- Experience working with and overseeing CROs and external vendors.
- Proven ability to build strong relationships with investigators, site personnel, and cross-functional stakeholders.
- Ability to travel domestically and internationally up to 50%.