Global Clinical Trials Coordinator
1 day ago
A highly skilled professional with experience in clinical operations is sought by ICON to coordinate global clinical trials. The ideal candidate will have a strong understanding of trial management, excellent organizational skills, and the ability to work independently in a dynamic environment. As a Global In-House CRA, you will play a vital role in shaping the future of clinical development at ICON.
Main Responsibilities:
- Plan, execute, and report on clinical trials across various phases and therapeutic areas.
- Analyze and maintain accurate trial tracking systems, ensuring data integrity and compliance.
- Oversee budgeting and variance analysis, optimizing resource allocation and cost-effectiveness.
- Lead TMF management, ensuring seamless inspections and regulatory compliance.
- Develop expertise in IP and ancillary supply management, streamlining logistics and order fulfillment.
- Facilitate site and country feasibility assessments, regulatory document preparation, and review.
- Create and analyze key clinical trial data reports, providing actionable insights to stakeholders.
- Collaborate with team members to share knowledge, best practices, and mentorship opportunities.
Nice to Have:
- 2-3 years of experience in clinical operations, project management, or a related field.
- Advanced Excel proficiency, VLOOKUP, pivot tables, data analysis, and Microsoft Office.
- Proven track record of independent work, effective communication, and teamwork.
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