Clinical Research Coordinator I, Radiation Oncology
About The Position
Site: The Brigham and Women's Hospital, Inc. Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary This position works within the Clinical Research Program of the Department of Radiation Oncology and supports the research team in the overall conduct of clinical trials. We are seeking an energetic, organized, and detail-oriented individual to support a portfolio of multidisciplinary clinical research projects. The program leadership is committed to training and inspiring the next generation of healthcare leaders and clinicians, working on important clinical and healthcare issues—ranging from making the delivery of care safer and more efficient, to expanding health insurance coverage and eliminating disparities, to improving the performance of entire health systems. Provides assistance to the Principal Investigator and Study Team in coordinating research activities that may include conducting a variety of clinical research projects with established methodologies, data collection and management, and other research activities as assigned. This position is ideal for candidates planning to pursue medical or other graduate-level training. Applicants must be able to commit to a minimum of two years in the role.
Requirements
- Bachelor's Degree Science required
- Related post-bachelor's degree research experience 0-1 years required
- Ability to work more independently and as a team member.
- Computer literacy, analytical skills, and ability to resolve technical problems.
- Ability to interpret the acceptability of data results.
- Working knowledge of data management programs.
Responsibilities
- Assists with determining the suitability of study subjects and acts as a resource for patients and families.
- Has input into recruitment strategies and may contribute to protocol recommendations.
- Administers scores and evaluates study questionnaires.
- Maintains research data, patient files, regulatory binders, and study databases.
- Performs data analysis and QA/QC checks and organizes and interprets data.
- Assists with preparation for annual review and assists PI in completing study reports and presentations.
- May assist with training and orientation of new staff members.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
