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.
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. Working as a Clinical Study Assistant, exclusively assigned to a Pharmaceutical Company, you will perform tasks related to the planning and execution of clinical studies.
Key Responsibilities Include
Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with established protocols under the general supervision of the Functional Service Provider (FSP) Manager and in collaboration with the CTA Manager(s)
Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model
Perform departmental tasks as needed
Accountabilities
Review of study documentation, including essential document packets, study plans, informed consent forms
Supporting/oversight of risk-based monitoring
Attendance of key team meetings as required, including Minutes for selected studies
Supporting regulatory inspection readiness (e.g. SOP Lists, storyboard collation)
Support clinical trial systems (e.g. CTMS/TMF) and associated activities for selected studies
Supporting vendor contract administration as required
Support study close-out activities, e.g. financial reconciliation
Supporting additional ad-hoc activities as needed, as agreed with Manager(s)
Collaboration with internal departments (Legal, Insurance, R&D; fu