About the position
Job Description
Responsibilities
1. Assists in enrolling participants for clinical study, explaining
objectives, obtaining consent, recruiting and interviewing
participants. 2. Performs data collection and entry and tracks
consent forms or other related materials. 3. Prepares study
materials and assists in developing databases and pretesting data
collection input instruments. Generates basic recurring
materials/reports. 4. Assists in research project planning by
monitoring established project timeline. 5. Assists with developing
and recommending study procedures. 6. Assists with IRB submissions
and supporting documentation. 7. Assists in conducting literature
reviews by searching library or online services as directed. 8. May
guide and train data entry staff on data entry processes. 9. Can
serve as a liaison between project and participants and/or outside
groups.
Qualifications
Bachelor's degree in a related field; No experience is required
Except for qualifications established by law, additional related
experience and formal education in which one has gained the
knowledge, skills, and abilities required for full performance of
the work of the job class may be substituted for the education or
experience requirement on a year-for-year basis with 30 college
credits being equivalent to one year of experience. Employees in
this job class may be required to work with biohazardous or
radio-labeled materials and may be required to successfully
complete applicable safety training.
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