Medical Oncologist

Tennessee Oncology; Nashville (TN); On-site; USD 225,000 - 275,000; Full time

Benefits offered by this job

Top-Tier Compensation

Paid time off

CME reimbursement

Leadership opportunities

Partnership track

Job summary

Tennessee Oncology is looking for a Staff Medical Oncologist for the Phase 1 Drug Development Unit in Nashville. This full-time position involves study selection, patient enrollment, trial execution, and compliance with regulatory standards. Candidates with an MD/DO degree and experience in clinical trials are preferred. The role promises top-tier compensation with no cap on earning potential, a work-life balance, CME reimbursement, and opportunities for ownership. Contact at [e-mail].

Qualifications

• 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.

Responsibilities

• Responsible for study selection, patient enrollment, and study conduct.
• Monitor and analyze trial progress, outcomes, and safety data.
• Supervise the initiation, execution, and completion of multiple clinical trials.

Skills

Direct patient care

Clinical trial management

Scientific knowledge in oncology

Education

MD/DO degree

Job description

Medical Oncologist, Phase 1 Research Program Opportunity

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 trail 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. 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, & cutting‑edge technology

Contact: [e-mail]