Clinical Research Coordinator

Mass General Brigham•Boston, MA

1d•$21 - $29•Onsite

About The Position

The Clinical Nutrition Research Coordinator supports the development and implementation of a medically tailored meal (MTM) clinical trial at Massachusetts General Hospital and the Harvard T.H. Chan School of Public Health. This role combines clinical research coordination with hands-on food operations, including recipe development and standardization, meal preparation and packaging, and tracking participant dietary restrictions to support delivery of an MTM intervention. The position will contribute to building and operationalizing a scalable meal production and delivery pipeline for nutrition-based clinical interventions. Does this position require patient care? No direct patient care is required. However, the role will involve interaction with research participants for recruitment, dietary tracking, data collection, and meal coordination.

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

Assist with recipe development and standardization for study meals
Track ingredients and perform nutrient and calorie calculations as needed
Support meal preparation, portioning, packaging, labeling, storage, and shipping
Track participant dietary restrictions, food allergies, and individualized meal needs
Contribute to the development and maintenance of standard operating procedures (SOPs)
Support quality control processes and ensure intervention fidelity across study activities
Collaborate with a multidisciplinary research team across clinical and academic settings
Assist with documentation, organization, and coordination of clinical trial activities
Help with participant recruitment and research data collection
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.