Senior Director of Clinical Imaging

2 weeks ago

Cambridge, Cambridgeshire, United Kingdom ARTBIO Full time
Job Summary

We are seeking a highly skilled Senior Director of Clinical Imaging to join our team at ARTBIO. As a critical member of our Program Team, you will work closely with program leads, functional heads, and subject matter experts to advance our development pipeline.

Key Responsibilities
  • Develop Clinical Imaging Strategies: Design and implement clinical imaging strategies to support our clinical development plans for Radioligand Therapy (RLT) agents.
  • Imaging Protocol Development: Design and implement imaging protocols, plans, and procedures for clinical studies.
  • Medical Imaging Oversight: Provide oversight and guidance for all aspects of Medical Imaging for clinical trials.
  • Subject Matter Expertise: Deliver subject matter expertise regarding advanced imaging techniques, image evaluation, and dosimetry estimation.
  • Scientific and Technical Support: Provide scientific and technical support/oversight in research activities.
  • Technical/Radiological/Dosimetry Resolution: Manage the resolution of technical/radiological/dosimetry questions and issues on a study and program level.
  • Collaborations and Vendor Management: Facilitate imaging/dosimetry academic collaborations, contractors, vendor/partner interactions.
  • CRO Vendor Oversight: Oversee CRO vendors, including imaging core labs and dosimetry vendors, to ensure they optimally execute clinical imaging projects.
  • Team Collaboration and Performance: As a member of the oncology clinical team, ensure strong collaboration between functions, collaborators, and vendors and high team performance.
  • Program Development and Enhancement: Participate in program development/enhancement, financial planning and analysis, metrics and reporting, shared services relationship management, contract compliance, and process improvement.
Qualifications and Education
  • Industry Experience: At least 12 years of industry experience; advanced degree required, Ph.D. preferred, in Medical Physics or Radiation Protection.
  • Technical Competency: Demonstrate strong technical competency in medical imaging and dosimetry in the field of RLT development.
  • Regulatory and Clinical Research Experience: Experience in Medical Imaging, Regulatory and Clinical Research processes.
  • Direct Experience: Direct experience designing and managing imaging aspects of clinical protocols for oncology RLT agents, including study design, endpoint selection, dosimetry, harmonization between clinical sites, imaging core lab oversight, etc.
  • Imaging Study Design and Dosimetry Estimation: Specific experience with imaging study design and direct/indirect estimation of normal organ and tumor dosimetry for early-stage clinical development in RLT agents.
  • Interpersonal and Leadership Skills: Interpersonal skills, organization and communication skills, leadership skills, and problem-solving savvy.
  • Ability to Work Under Pressure: Demonstrated ability to work well under pressure.
  • Organizational and Time Management Skills: Strong organizational, planning, and time management skills.
  • Teamwork and Continuous Learning: Demonstrated ability to work well with team members and independently, and commitment to continuous learning and staying updated on industry trends and advancement.

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