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Northwestern Medicine·Lake Forest, IL

Clinical Research Coordinator

Healthcare AdministrationFull time
iPosting details
ScheduleFull time
RequirementsACRP or SOCRA certification. preferred
EducationBachelor's degree
Experience2+ years
SourceNorthwestern Medicine · posted Oct 5, 2026
✓Requirements
Certifications
ACRP or SOCRA certification. preferred
Education
✓Bachelor’s Degree in related field or equivalent experience in in lieu of a degree.
Qualifications
✓Two years’ experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice.
✓Intermediate computer and internet knowledge.
✓Excellent customer service and patient care skills.
✓Meticulous organizational skills.
✓Excellent demonstrated written and verbal communication abilities.
Three to Five years’ experience in clinical research trials. preferred
+Benefits
✓401(k) with match
✓Tuition assistance
+Northwestern Medicine
53administration roles open
Lake ForestIL · 29 mi to Chicago
Pay for this position
Employer-posted
$29.11 – $42.21/hr
Sign-on bonus
vs. Illinois administration roles that post payvs. IL administration rolesmedian $38.75
$15/hrTop of this range is 9% above the state median$75/hr
Apply to Northwestern MedicineContact Recruiter about this role
✓You’ll need
Certifications
ACRP or SOCRA certification. preferred
Education
✓Bachelor’s Degree in related field or equivalent experience in in lieu of a degree.
Qualifications
✓Two years’ experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice.
✓Intermediate computer and internet knowledge.
✓Excellent customer service and patient care skills.
✓Meticulous organizational skills.
✓Excellent demonstrated written and verbal communication abilities.
Three to Five years’ experience in clinical research trials. preferred
+Benefits
401(k) with matchTuition assistance

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About the role

Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinical Practice, standard operating procedures and sponsor requirements.