Medical Oncologist (Phase 1 Drug Development) - Tennessee Oncology

Medical Oncologist (Phase 1 Drug Development) - Tennessee Oncology

Job Summary

Occupation: Physician, Drug Development Unit/Phase 1 Research Program

Specialty: Hematology/Oncology

Clinic Location: Nashville, TN

Employment: Full-Time

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 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 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‑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

What We Offer

• Top‑Tier Compensation – No cap on earning potential
• Work‑Life Balance – Paid time off
• Professional Growth – CME reimbursement, leadership opportunities
• Partnership Track – Your path to ownership
• Research & Innovation – Access to clinical trials, conferences, and cutting‑edge technology