Study Coordinator

Where

Salt Lake City, UT

What you'll be doing

Responsible for assessing protocols and reviewing inclusion and exclusion criteria, the Study Coordinator will also assist in contract and payment terms negotiations, obtain informed consent and medical history and ensure proper collection and processing of specimens. Attendance and participation in staff and investigator meetings will also be expected.

What your background should be

IRB CITI Course in the Protection of Human Research subjects certificate to be obtained within six months of hire.

Required Schooling / Training

Bachelor's Degree in a related field or equivalent.

Who is the client company

Public co-educational space-grant research university in Salt Lake City.

If you are interested in this position, send your resume to apply@kochdavis.com