Position Title: Research Associate I
Position posting date: 12/3/20
Position start date: ASAP or until filled
Salary/Range: Dependent on Experience (DOE)
Status: Part Time (20 hours per/week), benefits eligible
Work Schedule: Monday – Friday, variable hours depending on needs of study
Job Code: JL 1184
Under supervision, performs various duties that require the use of manual, clerical, advising, public contact and/or analytical skills for safety and efficacy study for an industry category B investigation device. Responsible for identifying eligible study participants and coordinating the scheduling of study participant evaluation and follow-up. Speaks with potential study participants about the study procedures. Assesses inclusion and exclusion criteria as possible prior to consent using screening questions and clinical knowledge. Monitors and meets recruitment goals while assuring willing participation for all potential study participants. Administers informed consent process to interested potential study participants. Complies with safety and security policies and procedures. Processes specimens (coding, centrifugation, freezing) and ships to designated central lab. Extracts, logs, and codes data on demographic and clinical information including medical history, treatment, and outcomes. Enters data into electronic data capture system. Ensures compliance with IRB requirements. May perform other duties as assigned.
Bachelor's degree (BA/BS) in a related field and at least 6 months of related experience; or equivalent combination of education and experience.