RN Clinical Research Coordinator: Oncology Trials

PVH (Tommy Hilfiger/Calvin Klein); Indianapolis (IN); On-site; USD 34,205 - 63,534; Full time

Job summary

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator III (RN) to perform protocol coordination for oncology studies under PI supervision. The role requires working knowledge of GCP/ICH-FDA guidelines and experience handling adverse events, study drug dispensing, and regulatory documentation.

The ideal candidate holds a Nursing degree with 2–5 years of nursing experience (oncology preferred) and an active RN license, plus valid driver’s license for offsite meetings and

Qualifications

• Bachelor's or Associate degree in Nursing is required.
• Unencumbered RN license in state of employment.
• 2-5 years nursing experience; oncology preferred.
• Valid state Driver's License for travel to satellite offices/offsite meetings.

Responsibilities

• Coordinate care for patients on clinical research protocols per GCP/ICH-FDA.
• Review informed consent and discuss with subjects per SOPs.
• Maintain records of investigational products and study materials.
• Ensure data accuracy and regulatory compliance across the study.

Skills

GCP compliance

IRB/IEC knowledge

Data accuracy

Clinical trial coordination

Education

Nursing degree (Bachelor's or Associate)

Job description

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator III (RN) to perform protocol coordination for oncology studies under PI supervision. The role requires working knowledge of GCP/ICH-FDA guidelines and experience handling adverse events, study drug dispensing, and regulatory documentation.

The ideal candidate holds a Nursing degree with 2–5 years of nursing experience (oncology preferred) and an active RN license, plus valid driver’s license for offsite meetings and