Senior Clinical Trial Associate role at ICON supporting sponsor-dedicated clinical trial operations in Northern Ireland. Responsibilities include coordinating study teams, managing regulatory compliance, vendor coordination, and site performance tracking. Requires clinical research experience, bachelor's degree, and proficiency with trial management systems.
Responsibilities
- Plan and coordinate weekly team meetings, manage minutes, update slides and action logs
- Prepare and review regulatory documents ensuring GCP and regulatory compliance
- Support vendor management tasks including access requests, UAT coordination, and supply administration
- Track and analyze site performance metrics, provide efficiency reports to leadership
- Mentor junior staff and participate in training initiatives for clinical trial management
Requirements
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Clinical research experience in site management, monitoring, or equivalent roles
- Proficiency with systems including Veeva Vault, Excel, and vendor portals
- Strong project management and organizational skills for multiple priorities
- Excellent communication and interpersonal abilities with site personnel
- Regional-level clinical trial experience and analytical capabilities
- Legal right to work in Northern Ireland
Vacancy posted 16 days ago
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