Overnight Clinical Investigation Tech I Sleep Med PER DIEM

Mass General Brigham•Boston, MA

1d•Hybrid

About The Position

This position supports research studies in the Division of Sleep and Circadian Disorders. The role involves working independently under general supervision, using and troubleshooting specialized data collection devices, and interacting with study subjects. The primary shifts will be overnight, but may include combinations of day, evening, night, weekend, and holiday shifts. Responsibilities include instructing subjects on device usage, obtaining informed consent, collecting and analyzing research data, preparing regulatory documentation, creating REDCap surveys, and training students.

Requirements

Bachelor's Degree in a Related Field of Study required.
0-1 year of Research Related Experience preferred.
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

Using and troubleshooting specialized data collection devices during laboratory or outpatient studies.
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.
Creating REDCap surveys, questionnaires, and databases.
Training and scheduling students.
Interact with patients/subjects with regard to study.
Coordinates in-lab visits.
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.
Responsible for working with PI or post-doc to maintain and audit REDCap questionnaires and surveys, eConsents, and databases.