
Trial Coordinator Role
2 weeks ago
Participate in the execution of clinical trials as a Clinical Trial Assistant. This role involves providing administrative support, tracking study metrics, and coordinating various activities related to drug supply planning and vendor management.
Responsibilities include:
- Organizing meetings and taking minutes
- Tracking and updating study metrics
- Setting up and maintaining trial master files (TMF/eTMF)
- Assisting with budget and expense management
- Coordinating drug supply planning, provision, and destruction processes
- Managing trial equipment and materials
- Supporting vendors with printing, translation, and other services
Requirements:
- Previous experience as a Clinical Trial Assistant in the pharmaceutical or biotechnology industry
- Basic knowledge of essential documents, CFR, and GCP/ICH regulations
- Proficiency in using Microsoft Office, TMF, and CTMS systems
- Understanding of filing systems and organizational tools
- Bachelor's degree or equivalent preferred
What ICON Offers:
Competitive salary and benefits package
Annual leave entitlements
Range of health insurance options
Retirement planning offerings
Employee assistance program
Life assurance
Flexible country-specific benefits
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