Clinical Research Project Manager

To ensure efficient coordination of clinical trial activities, the full-time remote Clinical Research Project Manager will manage day-to-day operations of multi-center, PI-initiated trials, oversee regulatory submissions, and develop project management infrastructure while working independently within the Thoracic Oncology department. Key responsibilities Manage daily operations of assigned clinical trials, ensuring compliance with regulations and adherence to timelines Develop and maintain the Trial Master File (TMF), ensuring all essential documents are organized and compliant with Good Clinical Practice (GCP) standards Assist the Principal Investigator in developing protocols and consent forms, ensuring clarity and regulatory compliance Required qualifications Bachelor's Degree required, preferably in a field relevant to clinical research Three years of experience in clinical research or project management, ideally within multi-center oncology trials Basic understanding of clinical trial processes and regulatory requirements, including GCP guidelines Familiarity with trial management software, such as EPIC and OnCore Strong organizational skills to manage multiple tasks efficiently and ensure adherence to timelines