Sr Clinical Research Coordinator Sleep Medicine RL

Mass General Brigham•Boston, MA

1d•Hybrid

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. Working independently and 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 EKGs and anthropometry; maintaining and updating data generated by the study. Additionally, provide input into determining study subject suitability and input into recruitment strategy. A second set of responsibilities includes assisting with growth and maintenance of research data, including ensuring protocols and data elements are appropriately documented; this may include assisting with developing search, visualization, and harmonization tools.

Requirements

Bachelor's Degree Related Field of Study required
Related post-bachelor's degree research experience 3-5 years required
Ability to work more independently and as a team member.
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.
Able to display initiative to introduce innovations to research study.
Excellent time management, organizational, interpersonal, written, and verbal communication skills.

Nice To Haves

Graduate Diploma Related Field of Study preferred

Responsibilities

Independently determines the suitability of study subjects.
Develops and implements recruitment strategies.
Participates in the design of research methodology.
Plans, performs, and designs statistical analyses.
Recommends protocol changes, writes protocols, and contributes to manuscripts.
Independently performs specialized projects.
Recruiting, evaluating, and consenting patients for studies.
Collecting and organizing patient data.
Scheduling patients for study visits.
Performing clinical tests such as EKGs and anthropometry.
Maintaining and updating data generated by the study.
Assisting with growth and maintenance of research data, including ensuring protocols and data elements are appropriately documented.
Assisting with developing search, visualization, and harmonization tools.