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Research Site Monitor
hace 2 semanas
As a Clinical Research Associate at ICON, you will be part of a dynamic team dedicated to delivering high-quality clinical research services. Your primary responsibility will be to monitor the progress of clinical studies, ensuring they are conducted, recorded, and reported in accordance with established guidelines.
Main Responsibilities:
- Conducts site visits and remote monitoring activities to verify compliance with ICH-GCP guidelines and applicable regulations.
- Ensures the protection of study participants by confirming informed consent procedures and protocol adherence.
- Maintains accurate records and writes reports detailing site findings and updates tracking systems.
To be successful in this role, you will need to possess strong analytical and communication skills, with the ability to work independently and collaboratively as part of a team.
