Clinical Research Coordinator II

Mass General Brigham•Boston, MA

1d•$24 - $39•Onsite

About The Position

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. The Diabetes Research Center at the Massachusetts General Hospital seeks a highly motivated individual to assume the position of Clinical Research Coordinator (CRC) II. This individual will work as part of a dynamic and enthusiastic team of diabetes doctors, nurses, and educators, under the general supervision of the Research Center Nurse Director and Principal Investigator. This position offers the opportunity to work directly with research participants, nurses, and physicians and learn about clinical research in a large academic center. The Diabetes Research Center is dedicated to advance innovative and rigorous clinical research aimed at improving the diagnosis, prevention, and treatment of all forms of diabetes and its complications- ultimately leading to a cure.

Requirements

Bachelor's Degree Science required
Related post-bachelor's degree research experience 1-2 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.

Nice To Haves

Can this role accept experience in lieu of a degree? Yes

Responsibilities

Following established policies, procedures, and study protocols, 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.
Provides input into determining study subject suitability and input into recruitment strategy.
Performs data analysis, interpretation, QA/QC, and assists in completing reports and presentations.
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.