Clinical Research Coordinator

Mass General Brigham • Boston, MA

8d • $20 - $29 • Onsite

About The Position

The Brigham and Women’s Hospital Division of Cardiology is seeking a highly motivated and experienced individual for a Clinical Research Coordinator (CRC) I position to assist with ongoing and future clinical research studies involving patients with cardiac arrhythmias. The CRC I must be able to multi-task and work well with team members in a dynamic clinical research setting. The position is ideal for someone looking to collaborate with a dedicated group of medical professionals working to transform the way we care for patients with atrial fibrillation. The CRC I will gain invaluable experience in the field of research in Cardiology, Cardiac Arrhythmias, Atrial Fibrillation, ventricular tachycardia, implanted rhythm devices, and Catheter Ablation procedures, all in an academic clinical research setting. This is a full-time (40 hours/week) position; evening and weekend hours are rare but may be required to facilitate the conduct of the study. This position is fitting for someone interested in pursuing graduate studies or a career in the fields of medicine, public health, or clinical research. The highly motivated individual will participate in multicenter registry management and research. This individual will extensively review medical records to enroll patients at Brigham and Women’s Hospital in two large multicenter atrial fibrillation ablation registries with the potential for participation in additional research projects in the Cardiac Arrhythmia Section at BWH. The CRC I will set up research meetings among associated principal investigators, provide registry data entry, and participate in abstract and manuscript preparation.

Requirements

• Bachelor's Degree Related Field of Study required
• One year of relevant work experience.
• 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.

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
• Number of Employees: 5,001-10,000 employees