84181BR
Cardiology
Job Posting Description
Position Summary/ Department Summary:
This position works with Dr. Diego Porras, MD; Dr. Nicola Maschietto, MD, PhD; Dr. Brian Quinn, MD, and other physicians in the cardiac catheterization laboratory. Candidates who are enthusiastic about a commitment of at least two years are preferred.
Under general supervision, the Clinical Research Assistant in the Heart Center Clinical Research Program will coordinate daily operations of research studies. These may include but are not limited to:
- Cardiac Catheter Lab divisional research projects, including FDA\-regulated clinical trials for devices placed during cardiac catheterization procedures to treat congenital heart defects and other projects.
- The CRA will be responsible for patient outreach and recruitment, data entry, and general trial coordination.
- Institutional case contribution to a national external registry on cardiac catheterization and electrophysiology procedures to treat congenital heart defects.
- Supports the development, implementation, and tracking of clinical research studies, including patient recruitment and data collection in alignment with institutional policies.
- Assists Principal Investigators in study start up, regulatory preparation, and ongoing project tracking and implementation.
- Conducts accurate data collection through medical record review and maintains databases (e.g., REDCap), including data entry and cleaning.
- Prepares and submits IRB protocols, amendments, and continuing reviews; ensures compliance with human subject protection regulations and provides administrative support to studies and projects.
- Contributes to research outputs such as tables, figures, literature reviews, manuscripts, and other documentation.
- Maintains organized records, collaborates effectively, helps orient new staff, and escalates issues appropriately while meeting deadlines.
- A bachelor’s degree is required with background in university level science courses is preferred.
- Research skills, interest in learning new research skills, and the ability to work independently
- Excellent organizational and communication skills
- High attention to detail and the ability to keep meticulous records are required.
- Prior experience in clinical research and IRB preparation is a plus
- Knowledge of Microsoft Office and Zoom/Microsoft Teams and the ability to learn individual protocol\-specific software and web\-based systems (i.e., REDCap) are strongly preferred.
Key Responsibilities:
Minimum Qualifications
Education:
Experience:
Status
Full\-Time
Regular, Temporary, Per Diem
Regular
Standard Hours per Week
40
Pay Range
$41246\.40\-$61339\.20 Annual
Office/Site Location
Boston
Job Posting Category
Research
Remote Eligibility
Part Remote/Hybrid