Jobs at Ironwood Cancer and Research Centers

Assists with clinical trial operations, including regulatory file maintenance, data entry, CRF completion, query resolution, lab processing, study drug accountability, and compliance with protocols, federal regulations, and good clinical practices. Supports research nurses, monitoring and audit visits, staff orientation, and ongoing education. The role is full-time and onsite in Scottsdale.

Provide outpatient oncology nursing care across infusion centers, including chemotherapy and infusion treatments, patient monitoring, reaction intervention, accurate EMR documentation, safety compliance, and coordination across varying clinic environments. The role requires strong clinical judgment, adaptability, communication, and travel between locations.

Provides oncology nursing care across infusion centers in Scottsdale, Phoenix, and Dobson. Administers chemotherapy and infusion treatments, monitors patients for reactions, documents care in EMR systems, follows safety protocols, and adapts to varying clinic workflows. Requires an active Arizona RN license, oncology certification, CPR certification, a driver’s license, and the ability to travel between locations.

Manages and coordinates oncology clinical trials, including feasibility reviews, participant screening, consent, enrollment, clinical monitoring, investigational product administration, regulatory documentation, adverse event reporting, data entry, query resolution, and protocol compliance. Collaborates with investigators, research coordinators, regulatory staff, and sponsors while ensuring proper billing, drug accountability, randomization, blinding, and adherence to GCP and federal regulations.

Provide oncology nursing care across multiple infusion centers, including chemotherapy and infusion treatments, patient monitoring, reaction intervention, safety compliance, accurate EMR documentation, and patient education. The role requires adapting to different clinic environments, collaborating with care teams, and traveling between Central and East Valley locations. Candidates must hold an active Arizona RN license, ONS Chemo/Bio Certification or OCN certification, current CPR certification, and a valid driver’s license.

Supervise IV admixture pharmacy technicians and oversee sterile compounding operations in an oncology practice. Responsibilities include staffing, hiring, training, performance management, medication preparation, quality assurance audits, regulatory compliance, inventory control, purchasing, waste management, equipment tracking, and operational reporting. The role requires maintaining patient safety and aseptic standards while serving as a technical resource for pharmacy, nursing, and clinical staff.

Assists with clinical oncology trial operations, including regulatory file maintenance, data entry, CRF completion, query resolution, lab processing, study drug accountability, and audit or monitoring visits. Supports compliance with protocols, federal regulations, and good clinical practice standards. Helps maintain data quality, orient staff, and coordinate research documentation and logistics. The role is full-time, weekday daytime work in a clinical cancer research setting.

Provides outpatient oncology nursing care across infusion centers, including chemotherapy and infusion treatments, patient monitoring, reaction intervention, accurate EMR documentation, and adherence to safety protocols. Requires an active Arizona RN license, oncology chemotherapy certification or OCN credential, CPR certification, driver’s license, clinical judgment, adaptability, and travel between clinic locations.

Provides outpatient oncology nursing care across West Valley infusion centers in Goodyear, Surprise, and Glendale. Administers chemotherapy and infusions, monitors patients for adverse reactions, intervenes clinically, documents care in EMR systems, follows PPE and safety protocols, and adapts to varying clinic workflows and patient volumes.

Coordinates oncology clinical trials from feasibility through follow-up, including participant screening, consent, enrollment, protocol compliance, data and source documentation, adverse event reporting, regulatory file support, and patient assessments. Performs or schedules procedures such as blood collection, ECGs, vital signs, and specimen shipping while coordinating with investigators, research staff, IRB representatives, providers, and sponsors.

Manages and coordinates oncology clinical trials, including feasibility review, subject screening, consent, enrollment, monitoring, protocol compliance, regulatory documentation, adverse event reporting, data entry, query resolution, investigational product administration, and study drug accountability. Collaborates with investigators, research coordinators, regulatory staff, and sponsors while ensuring adherence to Good Clinical Practice, federal regulations, and study protocols.

Provides outpatient oncology nursing care across infusion centers, administering chemotherapy and infusions, monitoring patients for reactions, documenting in EMR systems, following safety protocols, and adapting to varied clinic environments. Requires an active Arizona RN license, ONS Chemo/Bio certification or OCN, CPR certification, and a driver’s license. Travel between locations is required.

Provide chemotherapy and infusion treatments to oncology patients across outpatient infusion centers. Monitor for treatment reactions, intervene appropriately, document care in EMR systems, follow PPE and safety protocols, and adapt to varying clinic workflows. Requires an active Arizona RN license, oncology chemotherapy certification or OCN credential, CPR certification, and a valid driver’s license. Travel between locations is required.

Provides outpatient oncology nursing care across infusion centers, including chemotherapy and infusion treatment, patient monitoring, reaction intervention, safety compliance, accurate EMR documentation, and compassionate patient support. Requires adaptability across clinic environments and travel between locations.

Oversee clinical trial financial operations, including budget reviews, sponsor contract negotiations, invoicing, collections, payment reconciliation, vendor invoice compliance, and CTMS financial workflows. Partner with investigators, research staff, sponsors, and finance teams to support study activation, billing compliance, reporting, onboarding, regulatory initiatives, and process improvements.

Coordinates oncology clinical trials across clinical and regulatory functions. Acts as liaison among investigators, study staff, providers, IRB, and sponsors; screens, consents, enrolls, and follows subjects; maintains source documentation and regulatory files; reports adverse events; manages randomization and blinding; and performs protocol-required procedures such as blood collection, ECGs, vital signs, and assessments.