Clinical Lead II

Role: Clinical Lead II responsible for site management, monitoring quality assurance, and overseeing clinical operations in rare disease and oncology trials. Objectives include ensuring audit readiness, monitoring data quality, and managing site performance improvements. Responsibilities involve serving as primary contact for site concerns, providing status updates during sponsor calls, overseeing monitoring deliverables through dashboards, tracking metrics such as data entry and protocol deviations, and supporting audit responses. Requirements include a bachelor's degree in a scientific or health-related field, minimum 2 years of clinical lead experience with onsite monitoring, and expertise in Risk-Based Monitoring. Therapeutic areas of focus are Rare Disease and Oncology. Preferred skills include strong leadership, organizational abilities, and knowledge of clinical financials. High-value biopharma specifics involve experience in rare disease and oncology clinical trials, site oversight, and quality management. Collaboration primarily with sites and internal teams, with no specific reporting line specified. The role is based at an unspecified location with no travel requirements detailed.