Location
McHenry, IL, United States
Posted
July 13, 2026
Job Description
Clinical Research Coordinator II – Oncology
Ability to travel between McHenry, Huntley, and Lake Forest Sites
Required Qualifications
Bachelor’s degree in health science, biological science, nursing, or related field
MUST HAVE 3+ years of clinical research experience
MUST HAVE phlebotomy, EKGs, vitals, and specimen processing experience
MUST HAVE experience with:
+ Patient recruitment and enrollment
+ Study protocols
+ EMR and EDC systems
+ Sponsor or investigator-initiated studies
+ Oncology clinical trial experience
+ Experience working directly with sponsors and monitors
+ Knowledge of FDA regulations, ICH-GCP, and IRB processes
+ CCRC, CCRP, SOCRA, or similar certification
Responsibilities
+ Coordinate clinical trials in compliance with protocols, GCP, HIPAA, FDA regulations, and institutional policies
+ Screen, recruit, consent, and enroll study part...
Ability to travel between McHenry, Huntley, and Lake Forest Sites
Required Qualifications
Bachelor’s degree in health science, biological science, nursing, or related field
MUST HAVE 3+ years of clinical research experience
MUST HAVE phlebotomy, EKGs, vitals, and specimen processing experience
MUST HAVE experience with:
+ Patient recruitment and enrollment
+ Study protocols
+ EMR and EDC systems
+ Sponsor or investigator-initiated studies
+ Oncology clinical trial experience
+ Experience working directly with sponsors and monitors
+ Knowledge of FDA regulations, ICH-GCP, and IRB processes
+ CCRC, CCRP, SOCRA, or similar certification
Responsibilities
+ Coordinate clinical trials in compliance with protocols, GCP, HIPAA, FDA regulations, and institutional policies
+ Screen, recruit, consent, and enroll study part...