Clinical Research Coordinator

Mass General Brigham•Boston, MA

1d•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. Our lab investigates the role of sleep-in surgical outcomes, with a particular focus on how sleep patterns and sleep health are associated with reducing the risk of postoperative delirium in older adults. The Clinical Research Coordinator (CRC) will support all aspects of clinical trial management, participant engagement, and data integrity. This role offers the opportunity to contribute to high-impact research at the intersection of sleep medicine, anesthesiology, and cognitive health. Following established policies, procedures, and study protocols, the Clinical Research Coordinator 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.

Requirements

Bachelor's Degree in health sciences, psychology, neuroscience, or related field required (experience can be accepted in lieu of a degree).
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

Some relevant research project work (0-1 year preferred)
Experience with assessment tools (e.g., CAM, MoCA, MMSE) preferred
Comfort interacting with older adult surgical patients and their families 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.