Senior Clinical Research Associate — US Site Monitoring
Behavioral Health Market Context
Apply Nowvia Learn4Good
Qualifications
- •A Bachelor's degree in life sciences and a minimum of 3 years of monitoring experience are required
- •Applicants should be fluent in English and able to travel 60-80%
Responsibilities
- •This role focuses on site management, ensuring compliance with Good Clinical Practices (GCP), and fostering effective relationships with investigator sites to enhance the delivery of clinical trials
- •Responsibilities include monitoring site activities, resolving protocol-related issues, and supporting patient safety
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