Director, Drug Development Unit - Tennessee Oncology
Director, Drug Development Unit - Tennessee Oncology
Chattanooga, TennesseePosted 5d agoattending physician
Hematology/OncologyFull-time
Overview
- Location
- Chattanooga, Tennessee
- Practice
- Private Practice, Community Oncology · Clinical and research facility with Phase I drug development unit and ancillary services
Role summary
OneOncology is recruiting for a Hematology/Oncology role in Chattanooga, Tennessee (Private Practice, Community Oncology with Outpatient clinical and research oncology).
What the posting highlights
- Care setting: Outpatient clinical and research oncology
- Patient population: Oncology patients enrolled in clinical trials
- Research or clinical-trial participation is noted
SalaryDr summary based on the original posting
Posted pay vs real comps
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Compensation
- Structure
- Productivity
Next steps
Employer
OneOncology
Verified employerHealthcare employer99 open roles
Trust state
Verified — claimed and engaged
EHR
Not provided
Source
Public ATS source (greenhouse)
Employer highlights
Improving the lives of everyone living with cancer.
Facility & Community
Chattanooga, Tennessee
Mapped from source coordinates
Facility details
- Practice setting
- Private Practice, Community Oncology
- Facility type
- Clinical and research facility with Phase I drug development unit and ancillary services
- Patient population
- Oncology patients enrolled in clinical trials
Community snapshot
Peer median
Building sample
Active supply
Tennessee
Full-time
Transparent pay
Not measured
SalaryDr source status
Work-life
Private Practice, Community Oncology
Improving the lives of everyone living with cancer.
Questions to ask the employer
- How is the productivity component calculated (wRVU rate, threshold, reconciliation cadence), and what did physicians here actually earn from it last year?
- What is the call schedule, and is call compensated separately or built into the base?
- How many weeks of PTO and CME time are included, and is unused time paid out?
Generated from this posting's disclosed facts and the SalaryDr comparison — bring them to the first recruiter call.
Work Design
- Inpatient / outpatient
- Outpatient clinical and research oncology
- Admin burden
- High administrative and leadership responsibilities including oversight of clinical trials, regulatory compliance, and team management
- FTE
- 1
- Research
- Yes
Visa & Eligibility
- Remote
- No
Source & Verification
- Source
- Public ATS source (greenhouse)
- First seen
- 5 days ago
- Last verified
- today
- Extraction confidence
- 85%
Full description
Director, Drug Development Unit
Tennessee Oncology
Chattanooga, TN
Job Details:
Occupation: Director, Drug Development Unit
Specialty: Hematology/Oncology
Clinic Location: Chattanooga, TN
Employment: Full-Time
Opportunity: Unique opportunity to blend clinical and research responsibilities
Board Certifications: BE/BC
Degree: MD/DO
Work Environment: Private Practice
Ideal Candidate: Board-Certified/Board-Eligible, strong background in providing direct patient care and conducting research
About the Practice and their Mission:
Tennessee Oncology is built on a foundation of clinical excellence, compassionate support, and commitment to helping our patients through exceedingly challenging times in their lives. The education and experience of our physicians and healthcare team enable us to provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their homes. The practice offers Hematology/Medical Oncology, Radiation Oncology, Palliative Care, and Clinical trial & Research Programs.
Tennessee Oncology is a proud partner of OneOncology. OneOncology is a national partnership of leading independent community oncology practices working together to improve the lives of everyone living with cancer with a physician-led, data-driven, technology-powered, and patient-centric model. Through OneOncology, partner practices have shared technology platforms that foster communication, data sharing, and clinical excellence across the network. OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices.
Practice Details:
- Total Group Count: 105 Physicians and 105 APPs
- Phase 1, 2, and 3 clinical trials
- Ancillary services include: in-house lab, in-house pathology, infusion centers, genetic counseling, proton therapy, imaging, retail pharmacy, nutritionist, physical therapist, social workers, chaplain
- Medical services include: hematology/medical oncology, radiation oncology, palliative care, and APPs
About the Role:
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. More job details below:
- 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.
- 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.
Recruitment Package:
- 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
- Become part of Physician-Led Organizations that Supports Work/Life Balance
If you would like to apply or learn more about this opportunity, please email your CV to shanna.carpien@oneoncology.com
I look forward to speaking with you!