Medical Oncologist (Phase 1 Drug Development) - Tennessee Oncology

OneOncology•Nashville, TN

9d•Onsite

About The Position

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.

Requirements

MD/DO Degree
BE/BC in Hematology/Oncology
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

Nice To Haves

Experienced Physicians preferred
Fellows encouraged to apply

Responsibilities

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