Clinical Research Coordinator I

Mass General Brigham • Boston, MA

6d • $20 - $28 • Onsite

About The Position

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. We are hiring a dedicated and detail-oriented Clinical Research Coordinator to help coordinate the CMIST trial (Contrast-Enhanced Mammography Imaging Screening Trial) at our academic Breast Imaging practice. The Contrast Mammography Imaging Screening Trial (CMIST) is a breast cancer screening study comparing two types of mammography, primarily for women with dense breast tissue. The work will be done at the Department of Radiology of Massachusetts General Hospital (MGH) at the main campus in the Avon Breast Center. Work will be performed under direct supervision of the local Principal Investigator (PI), a practicing radiologist. The Clinical Research Coordinator will serve a primary role involving all aspects of the CMIST study. Working independently but with supervision, she/he/they will be responsible for recruitment, scheduling and study documentation, as well as subject-oriented study procedures, preparing reports and performing administrative tasks as needed. There may also be an expectation to help with some clinical duties. The ideal candidate will possess strong organizational skills, a basic understanding of medical terminology, a comfort acting independently and proactively to run the trial and preferably, at least one year of experience in prospective clinical trials. Phlebotomy experience is also preferred. The job will begin in January 2026. Job Summary Summary Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Requirements

• Bachelor's Degree Related Field of Study required
• Careful attention to detail and good organizational skills.
• Ability to follow directions.
• Good interpersonal and communication skills.
• Computer literacy.
• Working knowledge of clinical research protocols.
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

• at least one year of experience in prospective clinical trials
• Phlebotomy experience is also preferred

Responsibilities

• Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
• Recruiting patients for clinical trials and conducting phone interviews.
• Verifies the accuracy of study forms and updates them per protocol.
• Prepares data for analysis and data entry.
• Documents patient visits and procedures.
• Assists with regulatory binders and QA/QC Procedures.
• Assists with interviewing study subjects.
• Assists with study regulator submissions.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level