Clinical Research Coordinator – Global Cancer Research & Training Program

Role Overview

• Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials)
• Ensure data quality and integrity throughout the life of the study
• Collaborate with research and care teams across MSK regarding data input
• Generate data reports and deliver them to all vital parties on the progress of the research project, database, or protocol
• Design and/or improve databases, data forms, and tools (e.g. patient/human subject calendars, schedules, tracking logs) to facilitate patient consent and specimen collection as needed for assigned research projects
• Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed
• Coordinate clinical research protocols and serve as the main point of contact, if applicable

Requirements

• Experience in clinical research, global health, healthcare operations, or other data-driven research environments preferred
• Experience working in global or cross-cultural team settings
• Familiarity with research databases, data entry, and/or data quality assurance; exposure to data management or basic analytics tools (e.g., Excel, R, or similar) preferred
• Proven ability to manage multiple concurrent tasks or projects in structured environments
• A 2-year commitment to the role is preferred

Benefits

• Annual international travel to Nigeria in support of global research and training activities