Senior Oncology Research Nurse Coordinator

Florida Cancer Specialists & Research Institute; Sarasota (FL); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Tuition reimbursement

401(k) match

Pet insurance

Legal insurance

Job summary

Florida Cancer Specialists & Research Institute in Sarasota is seeking a Research Coordinator to oversee oncology clinical studies under the supervision of the Principal Investigator and Research Director. You will ensure proper conduct, protocol adherence, and patient safety across study activities.

The role requires travel to investigator meetings, a valid RN license, and experience in oncology or clinical research.

Qualifications

• Candidates must have a valid RN license, in state of employment.
• Minimum of one year oncology or clinical research experience; or a minimum of five years combined oncology and clinical research experience.
• Effective communication skills, be organized, detail oriented, strong patient advocates.
• Candidates must be available to travel to investigators meetings.
• Valid Driver’s License, in state of residency, for travel to clinics.
• Must comply with the Company’s Driver Safety Operations and Motor Vehicle Records Check Pol

Responsibilities

• Responsible for the performance of the research study under the medical supervision of the PI and the research director.
• The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies.
• May provide coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III.

Skills

RN license

oncology experience

clinical research experience

communication skills

travel availability

driver's license

Job description

Florida Cancer Specialists & Research Institute in Sarasota is seeking a Research Coordinator to oversee oncology clinical studies under the supervision of the Principal Investigator and Research Director. You will ensure proper conduct, protocol adherence, and patient safety across study activities.

The role requires travel to investigator meetings, a valid RN license, and experience in oncology or clinical research.