Medical Oncologist, Phase 1 Research

Medical Oncologist Phase 1 Research Program Tennessee Oncology Nashville, TN Job Details Occupation: Staff Physician/Medical Oncologist, Drug Development Unit/Phase 1 Research Program Specialty: Medical Oncology Clinic Location: Nashville, TN Employment Full-Time 50% Clinic (general oncology - solid tumor) and 50% Research Limited Call Schedule and Inpatient Service Requirements Ideal Candidate Board-Certified/Board-Eligible Strong background in providing direct patient care and clinical trial management/support Prior PI and Sub-I experience in early and/or late phase clinical trials 0-5 years of prior experience About the Practice and their Mission Tennessee Oncology is built on a foundation of clinical excellence, compassionate support, and commitment to helping our patients through exceedingly challenging times in their lives. The education and experience of our physicians and healthcare team enable us to provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their homes. The practice offers Hematology/Medical Oncology, Radiation Oncology, Palliative Care, and Clinical trial & Research Programs. Tennessee Oncology is a proud partner of OneOncology. OneOncology is a national partnership of leading independent community oncology practices working together to improve the lives of everyone living with cancer with a physician-led, data-driven, technology-powered, and patient-centric model. Through OneOncology, partner practices have shared technology platforms that foster communication, data sharing, and clinical excellence across the network. OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices. Practice Details Total Group Count: 105 Physicians and 105 APPs Phase 1, 2, and 3 clinical trials Ancillary services include: in-house lab, in-house pathology, infusion centers, genetic counseling, proton therapy, imaging, retail pharmacy, nutritionist, physical therapist, social workers, chaplain Medical services include: hematology/medical oncology, radiation oncology, palliative care, and APPs About the Role Tennessee Oncology is seeking a Staff Medical Oncologist for the Phase I Drug Development Unit in Nashville. This role works with the Phase 1 Research Director and would be responsible for study selection, patient enrollment, study conduct, and sponsor relationships. The DDU is part of a larger Phase I research program within the Greco-Hainsworth Centers for Research at Tennessee Oncology, and part of a regional hub for clinical research based in Nashville, TN. Responsibilities include clinical trials infrastructure including study start-up, regulatory, contract and budgeting, data management, research nursing, pharmacy, patient management, adverse event monitoring, and quality. Responsibilities The role requires a high-performing and energetic individual who demonstrates outstanding scientific knowledge applicable to oncology clinical research and the highest personal and ethical standards. Support the Phase 1 director in developing the early phase portfolio and the program strategic vision. Design and review clinical trial protocols to ensure scientific rigor, ethical compliance, and patient safety. Supervise the initiation, execution, and completion of multiple clinical trials concurrently. Monitor and analyze trial progress, outcomes, and safety data to make data-driven decisions and adapt protocols as necessary. Ensure adherence to all relevant regulatory requirements and guidelines governing clinical trials in oncology. Establish and maintain ethical standards, obtaining necessary approvals from institutional review boards (IRBs) and ethics committees. Foster a collaborative environment among interdisciplinary teams, including physicians, researchers, research nurses, statisticians, data managers, and other relevant staff. Provide leadership, mentorship, and professional development opportunities for team members. Analyze trial results and data to draw meaningful conclusions and contribute to scientific publications and presentations at conferences. Prepare regular reports and updates on the progress and outcomes of clinical trials for stakeholders and governing bodies. Represent the organization in professional conferences, scientific meetings, and collaborations with industry partners and academic institutions. Ensure all processes, documentation, and procedures comply with quality assurance standards for clinical trials. Recruitment Package Highly Competitive Compensation Models, including Productivity/Quality Incentives Relocation Offered CME Reimbursement Comprehensive Medical/Dental Benefits Retirement Savings Plan Paid Time Off Offered Malpractice Coverage Paid Become part of Physician-Led Organizations that Supports Work/Life Balance #J-18808-Ljbffr