Clinical Research Coordinator I - Collaborative Center for XDP

Mass General Brigham•Boston, MA

21h•Onsite

About The Position

The General Hospital Corporation Mass General Brigham is a not-for-profit organization that relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts, to advance its mission. This mission encompasses patient care, research, teaching, and community service, with a commitment to providing exceptional care. The organization believes that high-performing teams drive groundbreaking medical discoveries and invites all applicants to join and experience being part of Mass General Brigham. The Clinical Research Coordinator I provides assistance on clinical research studies, adhering to established policies, procedures, and study protocols. Key responsibilities include recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy and EKGs; 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. This position does not require direct patient care.

Requirements

Bachelor's Degree in a Related Field of Study (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)

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.