Clinical Research Coordinator I

Mass General Brigham•Boston, MA

19h•Hybrid

About The Position

The Clinical Research Coordinator I (CRC I) will support programmatic and research activities under the direction of Michael Pistiner within the Mass General Hospital Food Allergy portfolio. This role spans two distinct but related initiatives: the Food Allergy Prevention Program and the Food Allergy Buddies Program. The Food Allergy Prevention Program focuses on early allergen introduction and caregiver education, including coordination of the Food Allergy Management & Prevention Support Tool for Infants and Toddlers (FAMP-IT), a digital clinical support and education platform. FAMP-IT is also used to provide education, training, and implementation support to state and local Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) offices and partners. The Prevention Program includes coordination of clinician- and caregiver-facing educational programming, including FAMP-IT Office Hours. The Food Allergy Buddies Program is a peer-support initiative designed to connect families managing food allergies and includes an associated research component evaluating program impact through a mixed-methods study. The CRC I will assist with day-to-day program operations, prevention programming, external partner coordination (including WIC stakeholders), participant engagement, clinical research activities, and grant development support. The role will also support ongoing review and updating of program and platform content to ensure alignment with current evidence and clinical guidelines. Strong organizational skills, attention to detail, and the ability to interact effectively with patients, families, community partners, and multidisciplinary teams are essential.

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.