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Chief Medical Officer,Radiotherapeutics

The University of Texas MD Anderson Cancer Center
Boston, MA Full Time
POSTED ON 1/25/2025
AVAILABLE BEFORE 4/23/2025

Job Title : Chief Medical Officer, Radiotherapeutics

Job Number : 35790

Location : Boston,MA

Job Description

The Consulting Chief Medical Officer (CMO) will provide strategic medical and clinical leadership to advance the company’s radiopharmaceutical pipeline. This role is advisory in nature, focusing on high-impact deliverables, including program strategy, Target Product Profile (TPP) development, regulatory strategy, and optimizing clinical trial design. The CMO will also play a key role in engaging with key opinion leaders (KOLs), interpreting translational research, and supporting fundraising efforts by articulating the clinical vision and potential of the company to investors and stakeholders.

Responsibilities

  • Define Clinical Strategy

Define and refine the clinical development strategy, including competitive landscape, and patient needs.

  • Provide strategic insights to guide indication selection and program prioritization.
  • Collaborate in developing Target Product Profiles (TPPs) that align with regulatory,
  • Clinical Research and Development Support :
  • Offer guidance on clinical trial design and execution, ensuring alignment with the latest scientific and medical advancements.

  • Analyze and interpret translational research to inform clinical strategy and decision-making.
  • Stakeholder Engagement :
  • Build and maintain relationships with key opinion leaders (KOLs), academic collaborators, and regulatory bodies.

  • Organize and lead advisory boards and investigator meetings to gather insights and optimize clinical strategies.
  • Collaborate with the executive team to communicate the clinical value proposition to investors and potential partners.
  • Provide medical and scientific expertise during fundraising discussions and due diligence processes.
  • Regulatory and Scientific Leadership :
  • Advise on the preparation and review of key regulatory documents, including briefing packages and clinical trial protocols.

  • Offer strategic input on regulatory submissions to achieve product approvals in key markets.
  • Required Skills

  • Education :
  • MD or equivalent degree; board certification in oncology, radiation oncology, or nuclear medicine strongly preferred.

  • Experience :
  • Minimum of 10 years in clinical development, with substantial expertise in oncology and / or radiopharmaceuticals.

  • Proven experience advising or leading early-stage companies in clinical and regulatory strategy.
  • Strong track record of engaging with KOLs and participating in investor and stakeholder communications.
  • Skills :
  • Expertise in clinical trial design, regulatory pathways, and translational research.

  • Exceptional communication and advisory skills, with the ability to convey complex medical concepts to diverse audiences.
  • Strategic thinker capable of balancing scientific rigor with business objectives.
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