• Perform site initiation, monitoring and close out visits in accordance with contracted scope of work, company SOPs and good clinical practices.• Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations under close supervision. Ensure accuracy, validity and completeness of data collected at investigational sites, which meet clinical objectives and protect patient safety. Escalate quality issues to trial manager..• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.