Research Enrollment Coordinator

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

The Mass General Brigham (MGB) Biobank is a prominent research program aimed at understanding how genes, lifestyle, and environmental factors influence people's health. Biobank Coordinators play a vital role in helping patients make informed decisions about participating in this research program. They assist in educating and recruiting patients from both outpatient and inpatient settings at Mass General Brigham (MGH). Biobank Coordinators are responsible for a variety of tasks, including educating patients with diverse levels of health literacy, obtaining consent, and thoroughly explaining consent forms and procedures to individuals from various cultural and educational backgrounds.

Additionally, they are tasked with entering and maintaining patient and survey data. Coordinators collaborate closely with physicians and clinic staff to ensure that recruitment activities are seamlessly integrated into clinic workflows. As the role evolves, duties may shift based on project demands, funding cycles, and the skill sets of other team members involved.

This position offers a unique opportunity to work in a dynamic clinical research environment, focusing on personalized medicine. It is well-suited for individuals pursuing careers in medicine, clinical research, and public health, and those specifically interested in genetic counseling, implementation medicine, and patient engagement.

High School Diploma or Equivalent required and Bachelor's Degree Health Administration preferred.

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Working in a healthcare or clinical research setting 1-2 years preferred.

• Knowledge of research methodologies, clinical trial processes, and regulatory requirements.
• Familiarity with Good Clinical Practice (GCP) guidelines and Institutional Review Board (IRB) procedures.
• Excellent interpersonal and communication skills to effectively interact with healthcare providers, researchers, and study participants.
• Strong attention to detail and organizational skills to manage participant enrollment and data collection.
• Ability to explain complex research protocols and procedures to potential participants in a clear and understandable manner.

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