Clinical Research Coordinator

Mass General Brigham•Boston, MA

28d•$21 - $29•Onsite

About The Position

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 (up to one year if starting on a per diem basis) to provide degree equivalency verification. Join the Corrigan Minehan Heart Center Clinical Program in Boston, MA as a full-time Clinical Research Coordinator supporting innovative cardiovascular clinical and translational research. You’ll be part of a collaborative, mission-driven team advancing cutting-edge therapies while gaining valuable experience in a fast-growing research environment. Highlights include: • Hands-on exposure to exciting cardiovascular clinical trials • Mentorship and learning opportunities with leading physician-investigators • Meaningful direct patient interaction and impact Key responsibilities may include: participant recruitment and enrollment, maintaining IRB/regulatory documentation, coordinating study finances, collaborating with sponsors and research partners, and managing research data, biospecimens, and day-to-day study operations.

Requirements

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.

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.
participant recruitment and enrollment
maintaining IRB/regulatory documentation
coordinating study finances
collaborating with sponsors and research partners
managing research data, biospecimens, and day-to-day study operations