Clinical Research Coordinator - CURT

Mass General Brigham • Somerville, MA

11d • Onsite

About The Position

The Center for Ultrasound Research and Translation (CURT) is a multidisciplinary translational research center that collaborates extensively with MGH clinicians, MIT scientists, and industry partners to leverage cutting edge diagnostic and therapeutic imaging tools to identify, quantify, and treat disease. Our broad mandate, to bring advances in imaging to the bedside, encompasses projects such as the development of non-invasive imaging biomarkers for chronic liver disease, the development of new image guided surgical robotic systems, and the creation of artificial intelligence image analysis/interpretation algorithms. At CURT, our work in academic science is intended to reach the clinic and have a tangible impact on improving human health. The Clinical Research Coordinator I (CRC I) is an integral member of the CURT team who will coordinate numerous administrative and compliance tasks to support the smooth operation of studies. Specifically, the CRC I will contribute to subject recruitment, study coordination and scheduling, and assisting with subject visits. The CRC I will also contribute to the maintenance of study records in accordance with IRB rules and regulations. Contributions to administrative, financial, and operational tasks will be required. We are seeking a highly motivated candidate who is eager to learn and work in a fast-paced environment and possesses strong interpersonal and organizational skills, excellent attention to detail, and the ability to manage a variety of tasks. An ideal candidate will also have analytical skills, independent problem-solving capabilities, and a high level of professionalism.

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.

Nice To Haves

• 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.
• Highly motivated candidate who is eager to learn and work in a fast-paced environment.
• Analytical skills, independent problem-solving capabilities, and a high level of professionalism.

Responsibilities

• 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.
• 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.
• Contribute to subject recruitment, study coordination and scheduling, and assisting with subject visits.
• Contribute to the maintenance of study records in accordance with IRB rules and regulations.
• Contributions to administrative, financial, and operational tasks will be required.

Benefits

• Comprehensive benefits
• Career advancement opportunities
• Differentials, premiums and bonuses as applicable
• Recognition programs designed to celebrate your contributions and support your professional growth.

What This Job Offers

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