Clinical Research Coordinator BWH Emergency Medicine

Mass General Brigham • Boston, MA

5d • $20 - $28 • Onsite

About The Position

The Brigham and Women's Hospital, Inc. 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. The Division of Clinical Research at the Mass General Brigham Department of Emergency Medicine is looking for motivated individuals to support various ongoing clinical research projects, such as infectious disease, neurology, cardiovascular critical care, digital health, behavioral health emergencies, advanced care planning, point-of-care ultrasound (POCUS), and the use of artificial intelligence in medicine. Responsibilities include screening, recruiting, and conducting study procedures in emergency departments, inpatient units, ICUs, endoscopy suites, and outpatient facilities. The role will involve rotating between Brigham and Women's Hospital, an academic medical center, and Brigham and Women's Faulkner Hospital, a community hospital. Some overnight shifts may be required based on study protocols, and weekend coverage will be needed about once a month. This position is well-suited for those interested in graduate studies or a career in medicine, public health, or clinical research, offering significant patient interaction as part of a clinical research team. Please submit your (1) resume, (2) cover letter, and (3) transcript. Address your cover letter to MGB EM Director of Clinical Research. Your cover letter should include at least the following: - Career aspirations - Earliest start date - Time commitment (e.g. two years) - Experience in patient care/interaction Job 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.; maintaining and updating data generated by the study. Does this position require Patient Care? No

Requirements

• Bachelor's Degree Science 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.

Nice To Haves

• EMT preferred
• Bilingual in Spanish and English preferred (proficiency will be assessed)

Responsibilities

• Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.
• Recruiting patients for clinical trials, conducts phone.
• 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