Clinical Research Coordinator I

Mass General Brigham•Boston, MA

1d•$21 - $29•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. The Alcohol-Associated Liver Disease (ALD) Program in the Division of Gastroenterology at Massachusetts General Hospital is seeking a full-time Clinical Research Coordinator for NIH-funded clinical trials of behavioral interventions for patients with alcohol use disorder (AUD) and liver disease. Working directly with Dr. Wei Zhang and a multidisciplinary team of hepatologists, addiction specialists, psychologists, social workers, and nurses, the coordinator will be the primary point of contact between the study and its participants — recruiting, consenting, and retaining patients, and managing data collection, regulatory activities, and study operations.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
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

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.

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.
Recruiting, consenting, and retaining patients.
Managing data collection, regulatory activities, and study operations.