Clinical Trial Associate - Office-based (Hybrid)
About this role
Clinical Trial Associate - Office-based (Hybrid)
What You Will Do Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include
- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
- Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
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