Clinical Research Coordintor

Mass General Brigham•Boston, MA

4d•Onsite

About The Position

The Clinical Research Coordinator in the Reproductive Endocrine Unit (REU) at Massachusetts General Hospital will work on studies of fertility/infertility and reproductive endocrinology. 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. The role involves screening and recruitment of individuals for study participation, ensuring protocol requirements are met, collecting data for input into the research databases, performing phlebotomy and vital signs assessments, handling biological samples, and maintaining and updating regulatory documentation for compliance. 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.

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.
Screening and recruitment of individuals for study participation.
Ensuring protocol requirements are met.
Collecting data for input into the research databases.
Performing phlebotomy and vital signs assessments.
Handling biological samples.
Maintaining and updating regulatory documentation for compliance.