Overnight Clinical Investigation Tech I Sleep Med PER DIEM
About The Position
Up to 20 hours/week. 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 overnight 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. -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. -This includes IRB applications, amendments, and continuing reviews, study standards of practice. -Responsible for working with PI or post-doc to design and create REDCap questionnaires and surveys, eConsents, and databases. -Trains personnel in the use of REDCap.
Requirements
- Bachelor's Degree Related Field of Study required
- Research Related Experience 0-1 year 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 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 design and create REDCap questionnaires and surveys, eConsents, and databases
- Trains personnel in the use of REDCap
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
