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Medical Oncologist (Phase 1 Drug Development) - Tennessee Oncology

External
oneoncology logoOneoncology · Nashville, TN
Full-timeOn-site3w ago
BudgetingClinical TrialsComplianceDocumentationLeadership
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About the role

Tennessee Oncology is seeking a Staff Medical Oncologist for the Phase 1 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 sponsorship relationships. The DDU is part of a larger Phase 1 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. 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-drive 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 About Nashville, TN Nashville, located in the heart of Tennessee, is a vibrant city known for its rich music heritage, thriving culinary scene, and welcoming Southern charm. As one of the fastest-growing metros in the U.S., it offers a dynamic mix of career opportunities, cultural attractions, and outdoor activities. From live performances on Broadway to scenic parks and greenways, Nashville provides an energetic yet balanced lifestyle that makes it an ideal place to live and work.

Benefits

Top-Tier Compensation - No cap on earning potentialComprehensive Benefits - Medical, Dental, Vision, Disability, LifeRetirement Plan - Secure your futureWork-Life Balance - Paid time offProfessional Growth - CME reimbursement, leadership opportunitiesPartnership Track - Your path to ownershipResearch & Innovation - Access to clinical trials, conferences, & cutting-edge technologyAbout the PracticeHealth insuranceDental insuranceVision insurance

Additional Information

Medical Oncologist, Phase 1 Research Program Opportunity Tennessee Oncology Nashville, TN Job Summary Occupation: Physician, Drug Development Unit/Phase 1 Research Program Specialty: Hematology/Oncology Clinic Location: Nashville, TN Employment: Full-Time Setting : Private Practice, Outpatient/Inpatient Board Certifications: BE/BC Degree: MD/DO Ideal Candidate: Experienced Physicians preferred; Fellows encouraged to apply Strong background in providing direct patient care and clinical trail management/support Prior PI and Sub-I experience in early and/or late phase clinical trials 0-5 years of prior experience


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