Overnight Clinical Investigation Tech I Sleep Med PER DIEM

Mass General Brigham•Boston, MA

9h•Hybrid

About The Position

Working independently and under general supervision of a Research Manager, Post-Doctoral Fellow, or Principal Investigator and following established policies and procedures, provides support to research studies being carried out in the Division of Sleep and Circadian Disorders. Using and trouble-shooting specialized data collection devices during laboratory or outpatient studies, which will primarily be during night shifts but may include combinations of day/evening/ night/weekend/holiday shifts. 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. This includes IRB applications, amendments, and continuing reviews, study standards of practice. Responsible for working with PI or post-doc to maintain and audit REDCap questionnaires and surveys, eConsents, and databases.

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

Using and trouble-shooting 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