Clinical Research Coordinator

Mass General Brigham•Boston, MA

2d•Onsite

About The Position

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. A research lab within the Brigham and Women’s Cardiovascular Medicine division is currently seeking a motivated, personable, and detail-oriented individual to carry out clinical research related to cardiovascular disease and wearable sensors. This position will work on a new project combining cardiology, pulmonology, and data science at Brigham and Women’s Hospital in collaboration with a multinational technology company. Working under the supervision of the Director of Operations & Senior Project Manager, the candidate will follow established policies and procedures to execute the studies. The Clinical Research Coordinator will be responsible for recruiting and evaluating patients for studies (both in-person and remotely), collecting and organizing patient data, maintaining and updating data generated by the study, and data analysis. Because much of the work is team-based, the candidate will closely collaborate with research assistants, project managers, clinicians, and data scientists. In some instances, the candidate may engage with our industry partners, fostering collaborative relationships that enhance the project’s scope and impact.

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.

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 and evaluating patients for studies (both in-person and remotely).
Collecting and organizing patient data.
Maintaining and updating data generated by the study.
Data analysis.