Senior Oncology Clinical Research Coordinator (RN)

American Oncology Management Company; Indianapolis (IN); On-site; USD 52,000 - 96,000; Full time

Job summary

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator III (RN) to oversee and coordinate patients in oncology trials. You will operate under medical supervision, ensure protocol adherence, and manage study procedures with high accuracy across complex trial designs.

Responsibilities include eligibility assessment, informed consent discussions, adverse event reporting, data integrity, and coordination with sponsors, IRB/IEC, and study team.

Qualifications

• RN license in state of employment or multi-state license.
• Bachelor's or Associate degree in Nursing.
• 2-5 years nursing experience; oncology experience preferred.

Responsibilities

• Coordinate care for patients on clinical research protocols per GCP/ICH and FDA guidelines.
• Review protocol elements, assess eligibility, and document subject data.
• Monitor and report adverse events; maintain study records and inventory.
• Ensure regulatory compliance, data integrity, and sponsor communications.

Skills

Critical Thinking

Interpersonal Skills

Communication

Customer Service

Self-Management

Multi-site Coordination

Education

Bachelor's or Associate degree in Nursing

Tools

EMR

EDC

CTMS

MS Office

Job description

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator III (RN) to oversee and coordinate patients in oncology trials. You will operate under medical supervision, ensure protocol adherence, and manage study procedures with high accuracy across complex trial designs.

Responsibilities include eligibility assessment, informed consent discussions, adverse event reporting, data integrity, and coordination with sponsors, IRB/IEC, and study team.