Clinical Research Coordinator I

Mass General Brigham • Boston, MA

22h • $20 - $29 • Onsite

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 Clinical Decision Technology Laboratory (CDTL), based in the Department of Emergency Medicine at Massachusetts General Hospital, is seeking a motivated individual to join the laboratory as a Clinical Research Coordinator (CRC). Reporting to the PI and Senior Clinical Research Program Manager, the CRC will support the APPRAISE 2.0 research trial. In this research study, we are evaluating the APPRAISE software system, which is designed to help clinicians keep track of the state of seriously injured trauma patients and the appropriate steps in managing their injuries. The APPRAISE software runs in real-time at the bedside of actual Emergency Department patients. This software was developed by the CDTL. Throughout this research project, the APPRAISE software system will be continually modified and improved. The CRC will help carry out the day-to-day activities of the investigational protocol. This will include directly interacting with patients and families of major physical traumas in obtaining informed consent, extracting data from chart review, visualizing and analyzing data, and supporting regulatory compliance of the trial. The CRC will also directly interact with APPRAISE 2.0 stakeholders, including trauma surgeons, emergency medicine physicians, and nurses. The CDTL is a tight-knit community of kind and thoughtful researchers who specialize in analyzing temporal data, developing clinical software, and performing clinical trials. One central question underlies our work: How can new technology enable emergency care that is safer, more effective, and more efficient? This position provides excellent experience for someone interested in applying to medical school or graduate school. Familiarity with medical terminology from other experience such as medical scribe or EMT is preferred. Working knowledge in coding and/or programming is valuable. Please submit your (1) resume, (2) cover letter, and (3) transcript. Address your cover letter to Director, Clinical Decision Technology Laboratory. Your cover letter should include at least the following: - Career aspirations - Earliest start date - Time commitment (e.g. two years) - Clinical and/or coding experience/skills 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.; 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 to provide degree equivalency verification.

Requirements

• Bachelor's Degree Science 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.
• Some relevant research project work 0-1 year preferred

Nice To Haves

• EMT certification is preferred
• Spanish proficiency is preferred
• Familiarity with medical terminology from other experience such as medical scribe or EMT is preferred.
• Working knowledge in coding and/or programming is valuable.

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