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.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Assist with drafting, publishing, and distributing recruitment materials
Screen potential subjects
Verify accuracy of study forms
Update study forms per protocol
Document patient visits and procedures
Assist with regulatory binders and QA/QC procedures
Organize and coordinate subject study appointments
Maintain logs of confidential study and subject data
Provide basic explanation of study and in some cases obtains informed consent from subjects
Assist with study regulatory submissions
Collect information and draft preliminary reports, memos
Collect, organize, and record data as required by protocols
Actively participate in meetings and teleconferences with other research colleagues
Conduct literature searches, manuscript review, and other research activities
Provide organizational and administrative support, including ordering supplies
Other duties as requested.
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
The position requires excellent organizational skills, attention to detail, computer literacy including email, database entry and management, strong interpersonal skills and the ability to work both as a team member and independently.
Personable, yet professional demeanor, good interpersonal skills needed to interact with potential volunteers or patients.
Ability to handle sensitive and confidential information with clear commitment to maintaining security and privacy protocols.
Strong computer skills, courses in statistics, prior experience with programming languages, preferred.
Prior research experience as part of college course work or employment in research setting, preferred.
Qualifications
EDUCATION:
Bachelor's degree required.
EXPERIENCE:
Required: Demonstrated experience interacting and communicating with people as volunteer, summer employment or part of academic activities.
Preferred: Prior experience in healthcare/research
WORKING CONDITIONS:
• Standard office (dry lab) environment; cubicle (day-to-day operations)
• Hospital unit may include inpatient areas, outpatient facility, procedural facilities, and research laboratories.
EEO Statement
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.
