Clinical Research Project Manager

Job Summary

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