Clinical Research Associate/Clinical Research Coordinator I - Remote

Overview

The Cancer Center Protocol Office at Mass General Brigham is seeking motivated individuals to join as Clinical Research Associate/Clinical Research Coordinator I, supporting clinical researchers in cancer studies by managing patient enrollment, data collection, and regulatory compliance.

In Short

• Join a centralized research office supporting clinical trials.
• Enroll eligible patients for cancer studies.
• Manage data collection and submission for multiple studies.
• Coordinate communication between clinical teams and IRB.
• Perform regulatory management and patient coordination.
• Assist in scheduling tests and procedures for patients.
• Maintain accurate research documentation and data entry.
• Monitor and report on study compliance and adverse events.
• Participate in training on clinical research regulations.
• Work primarily on-site with some remote work options.

Requirements

• BA/BS degree required.
• Strong attention to detail and organizational skills.
• Good communication abilities and computer literacy.
• Knowledge of clinical research protocols preferred.
• Ability to follow directions and demonstrate professionalism.

Benefits

• Opportunity to work in a diverse and inclusive environment.
• Engagement in meaningful work impacting patient care.
• Access to training and development in clinical research.
• Supportive team environment focused on collaboration.
• Potential for career growth within a leading healthcare system.