Clinical Research Study Assistant II - Pediatrics Hematology & Oncology
Position Summary
Under direction, participates in clinical research study activities; screens, obtains consent, and enrolls participants in study; performs a variety of duties involved in the collection, documentation, and reporting of clinical research data.
Job Description
Primary Duties & Responsibilities:
- Assists clinical research coordinators with management of clinical trials, including: screening, enrolling, preparing informed consent packets, extracting data accurately from source documents and reporting in various data entry systems within protocol specified deadlines, routinely ensuring timely completion of all protocol requirements.
- Assists clinical staff with consenting participants for non-therapeutic clinical trials; assists clinical staff in administering patient reported outcome surveys and other participant questionnaires.
- Assists with study sample tracking and shipping.
- Assists with other duties as assigned by research team.
Working Conditions:
Job Location/Working Conditions: Normal office environment.
Physical Effort: Typically sitting at desk or table. Repetitive wrist, hand or finger movement.
Equipment: Office equipment.
Required Qualifications
Education: High school diploma or equivalent high school certification or combination of education and/or experience.
Certifications: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross. Basic Life Support certification must be obtained within one month of hire date (Online Basic Life Support certifications, those without a skills assessment component, are not sufficient).
Work Experience: Administrative Or Research (2 Years)
Preferred Qualifications
Education: Associate degree
Skills: Interpersonal Communication, Oral Communications, Organizing, Written Communication
Grade
C07-H
Salary Range
$19.21 - $28.85 / Hourly
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