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Clinical Trials Coordinator
2 months ago
Clinical Research Coordinator at ICON Strategic Solutions
Position Overview:
The Clinical Research Coordinator plays a pivotal role in ensuring participant welfare while supporting the overarching goals of ICON as a premier site network.
Key Responsibilities:
- Facilitate the recruitment of qualified participants and maintain communication with sponsor representatives.
- Oversee and execute clinical studies in alignment with established protocols.
Detailed Job Functions:
- Enhance and uphold competencies to meet regulatory standards.
- Conduct initial study activities, including participant recruitment strategies and preliminary screenings.
- Maintain and update the Clinical Trial Management System along with study-related databases.
- Engage with the Clinical Operations Manager regarding training progress and recruitment updates.
- Participate in investigator meetings and ensure source documents are current.
- Gather study data and fulfill technical protocol obligations.
- Document laboratory findings and any adverse events in a timely manner.
- Foster strong relationships with Investigators and ensure ongoing communication.
- Administer study medications under the guidance of the Investigator.
- Interact with sponsors through various communication methods.
- Accurately input visit data and promptly address any inquiries.
- Report any protocol breaches or deviations to management.
- Build rapport with volunteers and provide comprehensive education regarding clinical trials.
- Support colleagues and proactively identify potential challenges.
- Prepare documentation for audits and assist auditors as required.
- Willingness to travel to various sites within the network may be necessary.
