Clinical Research Coordinator I

Mass General Brigham • Boston, MA

4d • $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 Musolino Laboratory in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. Our research group is a translational neuroscience laboratory spanning multiple neurodegenerative disorders with a focus on genetic vascular disorders that affect the nervous system. Job Summary The laboratory seeks an exceptional candidate to coordinate natural history studies under the Young Genetic Stroke Alliance (YGSA), MLIV Natural History Study, and ACTA2 Natural History Study. This support will expand research efforts at MGH and help move basic science efforts from bench to bedside. The clinical research coordinator will work very independently but receive some guidance and supervision from the Principal Investigator. The job requires high level time management and organizational skills. Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.

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; 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