Clinical Research Coordinator

Summary

Join our team as a remote Clinical Research Coordinator to provide clinical trial support to oncology clinics in the TIME network and ensure efficiency in Tempus TIME Trial operations.

Requirements

• Candidate must have a Bachelor’s degree in Life Sciences or a health related field
• 2+ years of clinical research experience in an oncology setting
• Knowledge of current FDA regulations, and Good Clinical Practices (GCP's) governing clinical research and HIPAA
• CCRC preferable
• Must be a self-starter who can work independently with minimal supervision
• Strong planning and project management skills, with the ability to set goals and prioritize/manage multiple projects and tasks
• Excellent organization and communication skills with high attention to detail
• Proficiency with EDC systems and database management
• Proficiency with MS Office applications (Word, Excel, PowerPoint)

Responsibilities

• Educate and provide status updates to physicians and research staff regarding clinical trials in the TIME program portfolio
• Oversee the Tempus generated patient matches and maintain the patient tracker
• Screen potential study participants for available TIME trials
• Prepare rapid study activations for just-in-TIME trials and assist as needed during start-up
• Ensure all clinical trial data is entered into electronic data capture (EDC) systems in a timely and efficient manner, adhering to established protocols and guidelines
• Participate in research meetings, molecular tumor boards and/or regular physician meetings to review patient cases related to TIME Trials
• Participate in the Tempus TIME site onboarding process and ensure start-up timelines are met
• Create site support tools and TIME trial related communications