Evening Clinical Investigation Tech Sleep Research PER DIEM

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. This position provides support to research studies being carried out in the Division of Sleep and Circadian Disorders. Up to 25 hours/week, evening shift.

Requirements

Bachelor's Degree Related Field of Study required
0-1 year preferred Research Related Experience
Excellent interpersonal skills.
Good oral and written communication skills.
Analytical skills and the ability to resolve technical or research problems and issues and to interpret the acceptability of data results.
Knowledge of research protocols.
Excellent organizational skills and ability to prioritize a variety of tasks.
Ability to demonstrate professionalism and respect for subjects rights and individual needs and ability to maintain positive working relationships with co-workers and work cooperatively with peers.

Responsibilities

Investigator and following established policies and procedures, provides support to research studies being carried out in the Division of Sleep and Circadian Disorders.
Instructing subjects on the use of study devices and materials.
Obtaining informed consent for screening and for specific studies.
Collecting, organizing, and analyzing research data generated by the study.
Preparing and updating regulatory documentation for studies.
Maintaining/auditing REDCap surveys, questionnaires, and databases.
Training and scheduling students.
Using and trouble-shooting specialized data collection devices during laboratory or outpatient studies.
Initiates and maintains contact with study participants.
Interact with patients/subjects with regard to study.
Coordinates in-lab visits.
Specialized equipment calibration.
Supporting and executing measurements of study parameters on human subjects while using specific equipment and assays during the in-laboratory, outpatient, or field portions of research protocols.
Prepares and maintains regulatory documentation for group.
This includes IRB applications, amendments, and continuing reviews, study standards of practice.
Responsible for working with PI or post-doc to audit and maintain REDCap questionnaires and surveys, eConsents, and databases.