Director, Drug Development Unit - Tennessee Oncology

OneOncology • Chattanooga, TN

13h • Onsite

About The Position

Tennessee Oncology is seeking a Director of a new Phase I unit in Chattanooga. The Director will be responsible for the scientific leadership of this drug development unit including study selection, patient enrollment, study conduct, and sponsor relationships. This Phase I unit is part of a larger Phase I program within the Greco-Hainsworth Centers for Research at Tennessee Oncology, and part of a regional hub for clinical research. The Director will be supported a robust clinical trials infrastructure including study start-up, regulatory, contract and budgeting, data management, research nursing, pharmacy, and quality. The role requires a high-performing and energetic individual who demonstrates outstanding scientific knowledge applicable to hematology or oncology clinical research and the highest personal and ethical standards.

Requirements

• Board-Certified/Board-Eligible
• MD/DO degree
• Strong background in providing direct patient care and conducting research
• Outstanding scientific knowledge applicable to hematology or oncology clinical research
• Highest personal and ethical standards

Responsibilities

• Develop and implement a strategic vision for the oncology clinical trials and research department aligned with the organization's broader medical and research goals.
• Collaborate with senior management to set realistic objectives, timelines, and budgetary allocations for research initiatives.
• 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, 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.
• Actively seek opportunities for collaboration and funding for oncology research.
• Ensure all processes, documentation, and procedures comply with quality assurance standards for clinical trials.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree