Clinical Research Coordinator (Neuroendocrine Unit)

Site: The General Hospital Corporation, Mass General Brigham relies on a wide range of professionals to advance our mission. As a not‑for‑profit, we support patient care, research, teaching, and community service. Job Summary Following established policies, procedures, and study protocols, the Clinical Research Coordinator will provide assistance on clinical research studies, including recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy and EKGs; 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 Essential Functions 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. Additional Job Details The Neuroendocrine Unit focuses on the neurohormone oxytocin in human physiology and pathophysiology and therapeutic potential in human disease, and the neurobiology of eating disorders and obesity. Specifically, the CRC will support a study investigating the cognitive and neural mechanisms of cognitive‑behavioral therapy (CBT‑AR) for avoidant restrictive food intake disorder (ARFID) in children and adolescents. This study is a randomized controlled trial investigating whether CBT‑AR reduces food avoidance by targeting the maladaptive thoughts that prevent trying new foods and hyperactivity of brain regions involved in fear processing. In addition to the responsibilities listed, the CRC will also administer clinical and psychological interviews (training provided); operate the MRI machine (training provided); review test results and data with the nurse practitioners, study clinicians, and the principal investigator to ensure protocol requirements are met; develop meeting agendas to report on study progress and guide discussion related to agenda topics and document meeting notes; and manage study supply inventory and long‑term storage of biological samples following institutional biosafety precautions. The CRC will be a resource for subjects and study staff and will serve as the primary contact for urgent clinical research related matters. There may be opportunities to assist with preparing data for abstracts, posters, or manuscripts. Key competencies include strong writing and analytical skills with the ability to anticipate, identify, and present solutions to resolve problems, working knowledge of clinical research protocols and electronic data capture systems, and experience in data collection, cleaning, and analysis using tools such as SAS, SPSS, R, and Excel. The CRC is expected to be able to manage multiple responsibilities simultaneously and shift priorities as needed and to work independently under supervision and as a team player. The CRC must be able to work on‑site during normal business hours with the flexibility to attend study visits that will occur during early mornings and may take place in late evenings and on weekends. Psychology major and child/adolescent experience preferred. Qualifications Bachelor’s Degree in a related field. 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. Job Details Remote type: Onsite. Work location: 50 Staniford Street. Scheduled weekly hours: 40. Employee type: Regular. Work shift: Day (United States of America). Pay range: $29.01 per hour (Grade 5). EEO Statement The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at View phone number on click.appcast.io. #J-18808-Ljbffr