Clinical Research Coordinator – Oncology Trials & Training

BHS; United States; On-site; USD 52,000 - 76,000; Full time

Job summary

Baptist Health in Lexington, KY seeks a Clinical Research Coordinator I to coordinate patient care under IRB approved protocol requirements. The CRC works with investigators and study staff to ensure protocol compliance, accurate documentation, adverse event reporting, and coordination of trial activities in collaboration with clinical teams.

Under limited supervision, the CRC will build knowledge of research processes, maintain regulatory compliance, and seek guidance from senior staff as

Qualifications

• 3 years of experience in clinical research or as a clinical trial coordinator.
• Oncology clinical experience is preferred but not required.
• ACLS/BLS training within 6 months of hire.

Responsibilities

• Coordinate patient care in compliance with IRB approved protocols.
• Collaborate with investigators, research staff and departmental stakeholders.
• Document changes in condition, adverse events, concomitant medications and protocol adherence.
• Ensure accurate documentation and reporting for study interventions.

Skills

EMR proficiency

Microsoft Office

Education

Technical Diploma or Degree/certification in biology, public health, pharmacy, or health related field

Job description

Baptist Health in Lexington, KY seeks a Clinical Research Coordinator I to coordinate patient care under IRB approved protocol requirements. The CRC works with investigators and study staff to ensure protocol compliance, accurate documentation, adverse event reporting, and coordination of trial activities in collaboration with clinical teams.

Under limited supervision, the CRC will build knowledge of research processes, maintain regulatory compliance, and seek guidance from senior staff as