Senior Director, Clinical Imaging

4 weeks ago

Cambridge, United States ARTBIO Full time
Job DescriptionJob DescriptionSalary:

Summary

We are seeking a Senior Director of Clinical Imaging will be expected to take on a highly visible role with internal and external stakeholders through development of the strategy and management of imaging for clinical protocols in ARTBIO’s Radioligand Therapy (RLT) clinical development programs. As a critical member of the Program Team, you will work closely with program leads, functional heads and subject matter experts to advance the company’s development pipeline.

 

Responsibilities

  • Develops clinical imaging strategies designed to support the clinical development plans for RLT agents
  • Designs and implement imaging protocols, plans and procedures for clinical studies
  • Provides oversight and guidance for all aspects of Medical Imaging for clinical trials.
  • Delivers subject matter expertise regarding advanced imaging techniques (including  PET/CT, SPECT, MRI, CT and other modalities as needed), image evaluation, and dosimetry estimation.
  • Provides scientific and technical supports/oversite in research activities.
  • Manages the resolution of technical/radiological/dosimetry questions and issues on a study and program level.
  • Leads imaging/dosimetry academic collaborations, contractors, vendor/partner interactions.
  • Oversees CRO vendors including imaging core labs and dosimetry vendors to ensure they optimally execute clinical imaging projects
  • As a member of the oncology clinical team, ensures strong collaboration between functions, collaborators, and vendors and high team performance.
  • Participates in program development/enhancement, financial planning and analysis, metric and reporting, shared services relationship management, contract compliance, and process improvement.

 

Qualifications & Education

  • At least 12 years of industry experience; advanced degree required, Ph.D. preferred, in Medical Physics or Radiation Protection
  • Demonstrate a strong technical understanding of and commitment to medical imaging and dosimetry in the field of RLT development
  • Experience of Medical Imaging, Regulatory and Clinical Research processes
  • 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.)
  • Specific experience with imaging study design and direct/indirect estimation of normal organ and tumour dosimetry for early-stage clinical development in RLT agents
  • Interpersonal skills, organization and communication skills, leadership skills and problem-solving competency
  • Demonstrated ability to work well under pressure
  • Strong organizational, planning, and time management skills
  • Demonstrated ability to work well with team members and independently
  • Commitment to continuous learning and staying updated on industry trends and advancement


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