
This senior-level role involves joining a well-funded biotech team focused on oncology clinical trials. The position requires managing site relationships and conducting remote or on-site monitoring visits to ensure protocol compliance, data accuracy, and subject safety. Key responsibilities include overseeing study start-up and close-out documentation, resolving site performance issues, and communicating with investigators regarding recruitment and regulatory matters. The opportunity is appealing due to the chance to wear multiple hats in a growing company with a strong drug pipeline, offering a flexible schedule and comprehensive benefits. The role requires approximately 30 to 40 percent domestic travel.











