Study Coordinator

ICON · Blue Bell +1 more

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Clinical OperationsPart-timeCompany career page

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Role summary

Clinical Study Coordinator role at ICON focused on designing and analyzing clinical trials while managing protocol execution, regulatory compliance, and cross-functional communication. The position involves overseeing study timelines, budgets, and data quality across investigative sites and sponsor partnerships.

What they're looking for

Bachelor's degree in a relevant scientific discipline
Proven clinical research experience as Study Coordinator or similar role
Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
Strong organizational and multitasking abilities
Excellent communication and interpersonal skills
Legal right to work in the United States

What you'll be doing

Collaborate with cross-functional teams to develop and implement clinical trial protocols
Coordinate and oversee clinical study execution while ensuring protocol and regulatory adherence
Manage study timelines, budgets, and resources effectively
Facilitate communication among investigative sites, sponsors, and internal teams
Monitor and ensure data accuracy and completeness through quality control activities

Privacy & handoff

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Date posted2 days ago

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