Clinical Research Coordinator

Mass General Brigham • Boston, MA

5d • $20 - $29 • Hybrid

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. The Division of General Internal Medicine at Massachusetts General Hospital (MGH) seeks a full-time clinical research coordinator to work on research studies that focus on improving food security, nutrition, and cardiometabolic health. The research spans several projects, such as an evaluation of a Medicaid program to provide food and housing resources for low-income patients and an intervention using behavioral economics strategies to implement an evidence-based nutrition ranking system within a large Boston-based food bank and affiliated food pantries. The clinical research coordinator (CRC) will be an integral part of the study team, working in close collaboration with other research coordinators and staff, including physicians, health policy researchers, epidemiologists, and dietitians. The CRC will engage in study management and logistics, recruitment, enrollment, and data collection by phone or in the community at food pantries. The CRC will work directly under the supervision of the Principal Investigators. This position is an excellent opportunity for those interested in gaining clinical and research experience related to health care, public health, social determinants of health, nutrition, health behaviors, and implementation science.

Requirements

• Bachelor's Degree Related Field of Study required
• 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

• Some relevant research project work 0-1 year preferred

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