Clinical Research Coordinator - Clinical Research (Oncology) - Full Time

Summary

Jupiter Medical Center is a healthcare organization providing world-class care and serving communities in Palm Beach County and the greater Treasure Coast. The Clinical Research Coordinator manages all functional aspects of oncology and hematology clinical research, including patient screening and enrollment, protocol-compliant care, data collection, regulatory documentation, and quality improvement.

Responsibilities

• Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol
• Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability
• In collaboration with physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings
• Responsible for accurate and timely data collection, documentation, data entry, and reporting. Schedules and participates in monitoring and auditing activities
• Maintains regulatory documents in accordance with JMC SOPs and applicable regulations
• Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research
• Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality
• Performs other duties as assigned

Skills

• Bachelor's degree in life sciences, or an equivalent combination of education and experience
• Minimum of 2 years experience as a Clinical Research Coordinator or relevant experience in the Oncology / Hematology field
• If none, required to obtain within 24 months of hire
• Strong ability to organize, prioritize and work independently
• BSN preferred
• CCRC or CCRP certification preferred

Qualifications

Must Haves

• Bachelor's degree in life sciences, or an equivalent combination of education and experience
• Minimum of 2 years experience as a Clinical Research Coordinator or relevant experience in the Oncology / Hematology field
• If none, required to obtain within 24 months of hire
• Strong ability to organize, prioritize and work independently

Nice to Haves

• BSN preferred
• CCRC or CCRP certification preferred