Location
Cambridge, MA, United States
Posted
July 25, 2026
Job Description
Clinical Study Associate Manager
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**What You Will Do:**
+ May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study
+ Contributes to risk assessment and helps identify risk mitigation strategies
+ Supports feasibility assessment to select relevant regions and countries
+ Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc.
+ Reviews site level informed consents and other patient-facing study start-up material...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**What You Will Do:**
+ May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study
+ Contributes to risk assessment and helps identify risk mitigation strategies
+ Supports feasibility assessment to select relevant regions and countries
+ Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc.
+ Reviews site level informed consents and other patient-facing study start-up material...