Oncology Clinical Research Coordinator: Impactful Trials

Jupiter Med; Florida; On-site; USD 70,000 - 90,000; Full time

Job summary

Jupiter Medical Center, a leading health care provider in Palm Beach County, Florida, seeks a Clinical Research Coordinator to manage all functional aspects of clinical research. The role includes screening patients for trial eligibility, obtaining informed consent, enrolling patients, and coordinating care under protocol requirements.

Responsibilities also cover data collection, regulatory documentation, monitoring activities, and staff education on research processes.

Qualifications

• Bachelor’s degree in life sciences or equivalent combination of education and experience.
• Minimum of 2 years experience as a Clinical Research Coordinator or relevant experience in Oncology/Hematology.
• CCRC or CCRP certification preferred; if none, required to obtain within 24 months of hire.

Responsibilities

• Screens potential patients for protocol eligibility; presents trial concepts and details; enrolls patients on protocol.
• Coordinates patient care in compliance with protocol requirements; may disburse investigational drug and provide patient teaching.
• Maintains regulatory documents in accordance with SOPs and applicable regulations; ensures accurate data collection and reporting.
• Schedules and participates in monitoring and auditing activities.
• Identifies quality and performance improvement opportunities and collaborates on action plans.
• Performs other duties as assigned.

Skills

Organization

Prioritization

Independent work

Education

Bachelor’s degree in life sciences

BSN preferred

Job description

Jupiter Medical Center, a leading health care provider in Palm Beach County, Florida, seeks a Clinical Research Coordinator to manage all functional aspects of clinical research. The role includes screening patients for trial eligibility, obtaining informed consent, enrolling patients, and coordinating care under protocol requirements.

Responsibilities also cover data collection, regulatory documentation, monitoring activities, and staff education on research processes.