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Clinical Research Coordinator-Per Diem

Eisenhower Health
Eisenhower Medical Center
On-siteUSD 37 / hour

About this role

About the Role The Clinical Research Coordinator-Per Diem coordinates and implements clinical research activities within Eisenhower Health's Oncology research program. This role supports protocol development, participant recruitment and follow-up, data collection and monitoring to ensure compliance with GCP, SOPs and regulatory requirements. What You'll Do

  • Demonstrates compliance with Code of Conduct and compliance policies, and takes action to resolve compliance questions or concerns and report suspected violations.
  • Recruits, educates, consents, schedules, and completes follow-up with patients/subjects.
  • Participates in the design, planning and conduct of clinical trials program and clinical research projects.
  • Performs pre-investigation, initiation and periodic monitoring visits to assure that the protocol, obligations, responsibilities, and regulations are established and followed.
  • Monitors subject records for quality, data integrity and compliance with regulations and organization’s standard operating procedures (SOP).
  • Assists in writing and/or auditing clinical reports.
  • Assists in developing protocols, case report forms, and informed consent documents.
  • Works closely and acts as a liaison between sponsors, Contract Research Organization (CRO) sites and other department staff members. What We're Looking For
  • Education: Bachelor’s degree in healthcare and/or related field; completion of following CITI Program courses: Good Clinical Practice (GCP) Course, Clinical Research Coordinator Foundations, Clinical Research Coordinator Advanced.
  • Preferred: Master’s degree.
  • Licensure/Certification: Preferred: ACRP CCRC or SOCRA CCRP Certification; certification required upon eligibility.
  • Experience: Required: Three (3) years current experience in acute care hospital, medical center, health system or related industry.
  • Preferred: Previous experience with clinical trials. Nice to Have
  • Master’s degree (preferred)
  • ACRP CCRC or SOCRA CCRP Certification (preferred) Compensation & Benefits
  • Salary: $37.00 per hour.
  • Schedule: Per Diem.
  • Benefits: Not specified in posting.

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