Medical Oncologist/Hematologist – Community Oncology + Clinical Trials | Partnership Track
Job at a glance
Job description
We are seeking a Board-Certified Hematology/Medical Oncology Physician to join a growing community-based oncology practice with an expanding clinical research program.
This opportunity is ideal for a physician who wants to combine high-quality patient care, clinical leadership, and meaningful involvement in clinical research.
The physician will evaluate and treat a broad range of hematologic and oncologic conditions while participating as an Investigator or Sub-Investigator on sponsored clinical trials, helping eligible patients gain access to emerging cancer therapies.
You will work alongside experienced physicians, nurses, pharmacy professionals, research coordinators, and other clinical staff in an integrated outpatient environment.
This is also an excellent opportunity for physicians interested in building a long-term career with a pathway toward partnership and ownership.
Job Responsibilities
Diagnose and manage patients with hematologic and oncologic conditions.
Develop individualized, evidence-based treatment plans.
Manage chemotherapy, immunotherapy, targeted therapy, hormonal therapy, and supportive treatments.
Provide medical oversight of outpatient infusion services.
Monitor treatment response, laboratory results, toxicity, and adverse effects.
Manage treatment-related complications and adverse events.
Coordinate multidisciplinary patient care.
Educate patients and families regarding diagnoses, treatment options, risks, and expected outcomes.
Participate in hospital consultation, rounding, and call coverage as assigned.
Clinical Research
Participate as a Principal Investigator, Sub-Investigator, or Investigator on sponsored clinical trials, as appropriate.
Identify and evaluate potential clinical-trial candidates.
Review protocols and assess patient eligibility.
Provide medical oversight of research activities and patient safety.
Evaluate and document adverse events and serious adverse events.
Collaborate with sponsors, CROs, Medical Monitors, and research coordinators.
Participate in Investigator Meetings, site initiation activities, monitoring visits, and audits.
Support clinical-trial enrollment, retention, and protocol adherence.
Maintain compliance with applicable regulatory, ethical, and study requirements.
Contribute to the continued growth of the clinical research program.
Qualifications
MD or DO from an accredited medical school.
Completion of Internal Medicine residency.
Completion of Hematology/Oncology fellowship.
Board Certification in Hematology and/or Medical Oncology.
Current, unrestricted Illinois medical license.
Eligibility for hospital privileges.
Eligibility for Medicare, Medicaid, and commercial payer enrollment.
Current DEA registration or eligibility to obtain.
Strong clinical judgment and communication skills.
Ability to work effectively within a multidisciplinary clinical and research environment.
Preferred:
Previous Principal Investigator or Sub-Investigator experience.
FDA-regulated clinical research experience.
Familiarity with ICH-GCP guidelines.
Community-based hematology/oncology experience.
Experience overseeing outpatient chemotherapy/infusion services.
Clinical trial recruitment, enrollment, or patient-retention experience.
Interest in developing or expanding a clinical research program.
Working Hours
Skills
Hematology
Chemotherapy
Immunotherapy
Clinical Research
Clinical Trials
Outpatient Infusion
Cancer Care
Patient Management
Multidisciplinary Care