Clinical Research Coordinator

Mass General Brigham • Boston, MA

12h • $20 - $28 • Onsite

About The Position

The Massachusetts General 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. The CRC I must be able to multi-task in a dynamic clinical research setting. The ability to work well in a team is a must. This is the ideal position for someone looking to work with a dedicated group of people to make new and enhanced medical device technology available to patients with an array of cardiac conditions. The CRC I will gain invaluable experience in the field of Cardiology in an academic clinical research setting. This is a full-time (40 hours/week) position; evening and weekend hours may occasionally be required to facilitate the conduct of the study. 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. The responsibilities may vary according to projects, but include the following:

Requirements

• Strong interpersonal and communication skills, including the ability to interact with patients and study subjects.
• Excellent attention to detail.
• Capability to work well independently and within a multi-disciplinary team.
• Ability to balance and prioritize multiple dynamic projects and commitments.
• Bachelor's Degree Related Field of Study required
• Some relevant research project work 0-1 year preferred
• 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

• Willingness to commit to at least two years in the position is preferred.

Responsibilities

• Screens, recruits, and enrolls study participants.
• Conducts study visits in accordance with approved protocols and regulatory requirements.
• Serves as a key study resource for patients and their families.
• Maintains IRB submissions, regulatory files, and all required trial documentation.
• Assists with quality assurance/quality control (QA/QC) activities, and supports audits as needed.
• Manages study invoices and patient care charges.
• Acts as a liaison between internal teams, external collaborators, and sponsors to ensure timely trial progress.
• Collects, organizes, and maintains research data, patient records, and study databases.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level