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Site Monitoring Professional
hace 1 semana
We are seeking a skilled Clinical Research Associate 2 to join our team in this exciting opportunity. As a Clinical Research Associate 2, you will be responsible for conducting site monitoring activities and ensuring compliance with regulatory requirements. You will work closely with investigative sites to ensure the successful completion of clinical trials.
Main Duties and Responsibilities- Conducts site monitoring visits to ensure adherence to the protocol and regulatory requirements.
- Reviews and verifies data collected from investigative sites to ensure accuracy and completeness.
- Ensures that study participants are protected and that informed consent procedures are followed.
- Identifies and escalates any deviations or issues identified during site monitoring visits to the project manager or other relevant stakeholders.
