Clinical Research Coordinator, Senior

Mass General Brigham•Boston, MA

1d•$55,712 - $82,014•Hybrid

About The Position

The Senior Clinical Research Coordinator will support projects related to chronic disease management (chronic kidney disease, hypertension, diabetes) in primary care and the use of digital health technologies, electronic health records (EHRs), and clinical decision support (CDS) to improve care for patients. Primary projects include: (1) evaluating real-world continuous glucose monitoring (CGM) adoption and outcomes in older adults with type 2 diabetes, and (2) designing and implementing clinical decision support tools to improve quality of care for patients with chronic kidney disease (CKD) and hypertension in primary care clinics. The coordinator will work independently to manage study operations, participant recruitment, data collection, and regulatory compliance. Excellent attention to detail, critical thinking skills, professionalism, and interpersonal skills are essential. Strong data management and analysis skills in a clinical research environment are required. Principal duties vary depending on project phases (information gathering, data collection, analysis, dissemination). The coordinator will support all activities associated with execution of research plans including Institutional Review Board (IRB) submissions, progress reports, manuscript preparation, and communication with participants, clinical sites, and collaborators. The coordinator will use REDCap and Excel to assist with data collection and analysis. The coordinator will support the creation of novel datasets from multiple sources including EHR data and CGM data.

Requirements

Bachelor's Degree in a related field of study.
3-5 years of related post-bachelor's degree research experience.
High degree of computer literacy and analytical skills.
Ability to identify both technical and non-technical problems and develop solutions.
Ability to interpret acceptability of data results.
Highly proficient data management skills and working knowledge of data management systems.
Excellent time management, organizational, interpersonal, written, and verbal communication skills.

Nice To Haves

Graduate Diploma in a related field of study.

Responsibilities

Manage study operations, participant recruitment, data collection, and regulatory compliance.
Support Institutional Review Board (IRB) submissions, progress reports, and manuscript preparation.
Communicate with participants, clinical sites, and collaborators.
Assist with data collection and analysis using REDCap and Excel.
Support the creation of novel datasets from multiple sources including EHR data and CGM data.