Clinical Research Coordinator I

Mass General Brigham • Boston, MA

17h • $20 - $28 • 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. We are seeking a highly motivated and organized individual to work on the clinical research projects in the laboratory of Dr. Andrew T. Chan, Chief of the Clinical and Translational Epidemiology Unit at MGH. The candidate will work collaboratively to coordinate clinical research projects supervised by the principal investigator and other investigators within the CTEU. He/she will be expected to navigate clinical interactions with physicians, clinical research staff, and study participants, and troubleshoot clinical issues independently with collaborative guidance from colleagues. The candidate will join our team of clinical research coordinators and researchers to screen and identify eligible participants, coordinate patient interactions during study visits, and collect and process biospecimens critical to the outcome of our trials. Job Summary Job Profile Summary Summary 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. 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. Does this position require Patient Care? No

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level