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OneOncology · 1 month ago

Director, Drug Development Unit - Tennessee Oncology

Chattanooga, TN

Full-time

Onsite

Director/Executive

Tennessee Oncology, a partner of OneOncology, is seeking a Director for their new Phase I drug development unit in Chattanooga, TN. The role involves scientific leadership in clinical trials, overseeing study protocols, patient enrollment, and ensuring compliance with regulatory standards.

Health CareOncology

Growth Opportunities

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

Qualification

Hematology/Oncology expertiseClinical trial managementRegulatory complianceScientific leadershipPatient safetyData analysisMentorshipCollaboration

Required

Board-Certified/Board-Eligible

Strong background in providing direct patient care and conducting research

MD/DO degree

Outstanding scientific knowledge applicable to hematology or oncology clinical research

Highest personal and ethical standards

Ability to develop and implement a strategic vision for the oncology clinical trials and research department

Experience collaborating with senior management to set realistic objectives, timelines, and budgetary allocations for research initiatives

Ability to design and review clinical trial protocols to ensure scientific rigor, ethical compliance, and patient safety

Experience supervising the initiation, execution, and completion of multiple clinical trials concurrently

Ability to monitor and analyze trial progress, outcomes, and safety data to make data-driven decisions and adapt protocols as necessary

Knowledge of relevant regulatory requirements and guidelines governing clinical trials in oncology

Ability to establish and maintain ethical standards, obtaining necessary approvals from institutional review boards (IRBs) and ethics committees

Experience fostering a collaborative environment among interdisciplinary teams, including physicians, researchers, statisticians, data managers, and other relevant staff

Ability to provide leadership, mentorship, and professional development opportunities for team members

Experience analyzing trial results and data to draw meaningful conclusions and contribute to scientific publications and presentations at conferences

Ability to prepare regular reports and updates on the progress and outcomes of clinical trials for stakeholders and governing bodies

Experience representing the organization in professional conferences, scientific meetings, and collaborations with industry partners and academic institutions

Ability to actively seek opportunities for collaboration and funding for oncology research

Knowledge of 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

Become part of Physician-Led Organizations that Supports Work/Life Balance

Company

OneOncology

OneOncology is a partnership of oncologists and industry leading experts driving the future of community-based cancer care in the US. It is a sub-organization of General Atlantic.

Founded in 2018