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Regional Cancer Center Navigation

Memorial Regional Cancer Center

Clinical Research Office

Scope of Service
The Clinical Research Department of Memorial Hospital offers a comprehensive clinical research service that includes the following:

  • Hoosier Oncology Group (HOG)
  • Cancer and Leukemia Group B (CALGB) affiliated with the University of Chicago
  • National Surgical Adjuvant Breast and Bowel Project (NSABP) Full Affiliate
  • Radiation Therapy Oncology Group (RTOG), affiliated with Washington University in St. Louis
  • Pharmaceutical Studies involving Oncology Research
  • Pharmaceutical Studies involving Non-oncology Research

Goals of the Research Department:

  • To provide access to state of the art clinical trial for patients in the community and surrounding region.
  • To provide accurate monitoring of patient and protocol while on clinical trial.
  • To provide clinical trials that meet the needs of the community and surrounding region.

The staff of the Research Office consists of the following people:

  • Clinical Manager
  • 6 Research Nurses
  • 6 Clinical Research Associates

Participation:

  • Medical Oncologists
  • Radiation Oncologists
  • Radiologists
  • Surgeons
  • Urologists
  • Neurosurgeons
  • Oncology Nursing

Patient population/customer group served:

  • People who are at high risk for cancer (family history or organ changes) and meet the eligibility requirements for a specific trial. i.e. Breast Cancer Prevention Trial.
  • Patients newly diagnosed with cancer.
  • Patients currently treated for cancer.
  • Family members or patients themselves seeking information on clinical trials.
  • Physicians inquiring about availability of clinical trials for their patients.
  • Health care professionals needing information on current treatment for cancer.
  • Patients that have current health problems that meet the guidelines of studies currently active. For example, patients with narrowing of arteries in the legs - a non-oncology condition.

Services provided:

  • Assessment of eligibility for a specific clinical trial
  • Complete patient monitoring while on trial
  • Monitoring of protocol
  • Collaborative care between physician, patient, and research nurse
  • Symptom management of clinical trial patient
  • Information for patients and family members