Jobs · Healthcare · Tennessee

Director, Drug Development Unit

OneOncology · Chattanooga, TN · 1 wk ago
HealthcareFull-time

About the role

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.

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.

Requirements

Board Certifications: BE/BC

Degree: MD/DO

Qualifications

Experience: Strong background in providing direct patient care and conducting research.

Skills

Scientific Knowledge: Applicable to hematology or oncology clinical research.

Benefits

Highly Competitive Compensation Models, including Productivity/Quality Incentives

Relocation Offered

CME Reimbursement

Comprehensive Medical/Dental Benefits

Retail Savings Plan

Paid Time Off Offered

Malpractice Coverage Paid

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

Pay

N/A

Schedule

N/A

Benefits

N/A

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