As a Clinical Research Associate II, you will be responsible for conducting site qualification, site initiation, interim monitoring, site management and close-out visits to ensure compliance with regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) guidelines.
Key Responsibilities
* Evaluate site performance and provide recommendations regarding site-specific actions.
* Maintain a working knowledge of ICH/GCP Guidelines, relevant regulations and company processes.
Requirements
* Bachelor's degree or RN in a related field or equivalent combination of education, training and experience.
* Demonstrated knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
* Excellent computer skills and ability to adapt to new technologies.