- Contribute to site initiation, monitoring, close-out and tracking of clinical trial documentation and follow-through at sites on assigned clinical projects in collaboration with Project Managers and/or Assigned Personnel. - Responsible for reviewing study site progress, maintain metrics on enrollment at site level milestones. - Perform study monitoring activities including but not limited to source document verification, data review and compliance, data query generation and resolution, and review of regulatory binder and deliverables. - Obtain and maintain essential documentation in compliance with ICH-GCP, procedural documents and local regulations both in the office and at site. - Prepare study monitoring reports and finalize the report within specified timeline. - Proactively identify study-related issues and escalate as appropriate. - Ensure compliance with company policies and procedures. - Perform other duties as assigned.