Clinical Research Coordinator BWH Emergency Medicine

Mass General Brigham • Boston, MA

2d • $20 - $28 • Onsite

About The Position

The Brigham and Women's Hospital (BWH) Department of Emergency Medicine's Division of Clinical Research is seeking a highly motivated individual to assist with ongoing and future clinical research studies on a Full-time basis. Through participation in a variety of federally funded and industry sponsored clinical research studies and trials, our division aims to find new and effective treatments for injuries and illnesses such as but not limited to infections, trauma, stroke, and cardiopulmonary disorders. The incumbent will work with a dynamic team of investigators and research staff to coordinate multiple studies performed in the emergency departments at BWH and Faulkner Hospital. Evening hours and weekend hours may be required. Studies may require staff to be on-call one weekend and 5 weeknights a month. The ability of the successful candidate to take call is preferred. This position is ideal for someone interested in pursuing graduate studies or a career in the fields of medicine, public health, or clinical research. It involves extensive patient interaction as a member of a clinical research team. 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.

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.

Nice To Haves

• EMT preferred
• Bilingual in Spanish and English preferred (proficiency will be assessed)
• The ability of the successful candidate to take call is preferred.

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