Clinical Study Lead (CTM II)

ICON · Warren, NJ +1 more

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Clinical OperationsFull-time$122k–$152kCompany career page

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Role summary

Clinical Trial Manager II role overseeing vendor management, site coordination, and protocol execution for clinical studies in a sponsor-dedicated model. Reports to ICON Strategic Solutions with responsibility for budget adherence, timeline management, and regulatory compliance across multiple trial phases.

What they're looking for

Undergraduate degree in clinical, science, or health-related field from accredited institution
5 years relevant experience including 3 years clinical trial management
Licensed healthcare professional such as registered nurse preferred
Fluent English reading, writing, and speaking ability
Legal right to work in United States

What you'll be doing

Oversee vendor performance including CROs, biometrics, labs, and eTMF systems for budget and timeline adherence
Develop and maintain vendor and site relationships throughout all trial phases
Coordinate site readiness activities including study materials, drug shipping approvals, and protocol training
Review CRO monitoring reports, eTMF documentation, and trial registry entries for compliance
Support financial management by reviewing and approving vendor and site invoices

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