Clinical Trial Associate
hace 3 semanas
Role Overview
As a Clinical Trial Associate at ICON, you will be part of a world-leading clinical research organization. This role involves supporting the Local Trial Manager and CRA to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution, and closing of clinical trials. You will be responsible for regulatory document review and approval, including site-specific Informed Consents. Ensuring trial-related activities are in compliance with GCO SOPs, policies, and local regulatory requirements.
Key Responsibilities
- Work with the Local Trial Manager and CRA to ensure overall site management and adherence to internal SOPs, policies, and local regulatory requirements.
- Maintain site-level protocol information in Trial Management Systems (e.g. CTMS).
- Ensure current versions of the required trial documents, trial-related materials, and supplies are provided to the investigational site within required timeframes.
- Provide current and complete documents requested by the IEC/IRB and HA.
- Distribute, collect, review, and track regulatory documents, agreements, and training documentation.
- Contribute to process improvement initiatives.
Requirements
- 1-2 years of experience in a clinical trial setting.
- A minimum of a BA degree.
- Strong knowledge of MS Office.
- Excellent organizational skills and ability to collaborate and handle multiple priorities within a matrix environment.
What ICON Offers
Our success depends on the quality of our people. We offer a range of benefits, including annual leave entitlements, health insurance, and retirement planning offerings.
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