Description
As a Clinical Trial Manager II at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
You will be responsible for overseeing vendors, developing strong relationships with sites, and ensuring continuity of relationships throughout the trial phases.
Key responsibilities include:
- Vendor oversight for adherence to budget, timelines, and organisational objectives
- Developing strong vendor and site relationships
- Obtaining and maintaining in-depth understanding of the study protocol and related procedures
- Coordinating and managing tasks to achieve site readiness
- Performing timely review of monitoring reports from CRO and associated deliverables
- Reviewing CRO eTMF/TMF to ensure adherence with standards and compliance with regulations
- Working with vendors to revise scope of service agreements, budgets, plans, and detailed timelines
- Supporting financial management of the study, including review and approval of site and vendor invoices
- Supporting risk management initiatives and audit/inspection activities
- Maintaining clinical trial registry entry/updates
- Providing mentorship/guidance to junior team members or cross-functional colleagues
Requirements:
- Undergraduate degree or its international equivalent in a clinical, science, or health-related field
- 5 years of relevant experience, including 3 years of experience in clinical trial management
- Fluent English and fluent in the language of the host country
- Hybrid role - office-based three days per week in Warren, NJ, Armonk, NY, or Cambridge, MA
ICON offers a competitive and comprehensive total rewards package, including:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities