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Clinical Imaging Director

10+ years
Not Disclosed
10 Dec. 13, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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About Telix Pharmaceuticals
Telix Pharmaceuticals is a rapidly growing radiopharmaceutical company with a global presence, headquartered in Australia with offices in Belgium, Japan, Switzerland, and the United States. Our mission is to harness the power of precision medicine through targeted radiation, improving the quality of life for patients with cancer and rare diseases. As part of our team, you’ll contribute to the international roll-out of our approved prostate cancer imaging agent and the development of our late-stage clinical portfolio addressing critical unmet needs.


Role Overview: Clinical Imaging Director – Nuclear Medicine Center of Excellence

We are seeking an experienced Oncology Clinical Imaging expert to join our Nuclear Medicine Center of Excellence (NMCOE), under the Division of Precision Medicine. In this pivotal role, you will design and execute imaging protocols, optimize and interpret imaging data, and support the advancement of Telix’s diagnostic and therapeutic radiopharmaceuticals. Working collaboratively with cross-functional teams, you will help shape the future of precision imaging in oncology and rare diseases.

Core Team Members:
You will collaborate closely with a Nuclear Medicine Physician, Radiation Physicist, and other key stakeholders across Clinical Operations, Biostatistics, and Program Leadership.


Key Responsibilities

  • Imaging Expertise: Develop and execute imaging study protocols and workflows to advance diagnostic and therapeutic radiopharmaceuticals.
  • Clinical Documentation: Author imaging sections of clinical study documentation and regulatory filings.
  • Data Oversight: Lead the design, analysis, and quality control of imaging data, ensuring accuracy and adherence to clinical standards.
  • Vendor Management: Oversee third-party vendors, including imaging CROs, ensuring deliverables meet quality expectations.
  • Collaboration: Work with global leads to implement advanced imaging approaches across clinical studies.
  • Site Engagement: Engage with investigators and visit sites to support imaging studies and compliance.
  • Regulatory Alignment: Maintain compliance with ICH/GCP guidelines and provide imaging-related insights for regulatory submissions.
  • AI/ML Initiatives: Contribute to imaging advancements using artificial intelligence and machine learning.
  • Strategic Contributions: Support business development, M&A activities, and medical affairs through imaging insights.

Education and Experience Requirements

  • Education: Bachelor’s degree in Biomedical Science, Imaging, or a related field (required).
  • Experience:
    • 10+ years in nuclear medicine with an oncology focus.
    • Proven experience in clinical development within pharmaceutical or biotechnology industries.
    • Strong expertise in imaging CRO management and clinical trial documentation.
  • Technical Skills:
    • Proficient in imaging analysis software for radiology and nuclear medicine.
    • Familiarity with regulatory guidelines and GxP compliance.

Key Skills and Competencies

  • Leadership: Ability to lead and influence cross-functional teams and external stakeholders.
  • Communication: Excellent interpersonal and negotiation skills.
  • Strategic Thinking: Strong understanding of the nuclear imaging and therapy market, coupled with innovative problem-solving capabilities.
  • Adaptability: Thrives in a dynamic, fast-paced environment.
  • Collaboration: Commitment to fostering inclusivity and teamwork across global teams.
  • Results-Oriented: Focused on achieving measurable outcomes while maintaining high ethical standards.

Why Join Telix?

At Telix, we are driven by a shared purpose: helping people with cancer and rare diseases live longer, better-quality lives.

  • Global Reach: Work with a unique, interdisciplinary team located around the world.
  • Inclusive Culture: We embrace diversity and create an environment where everyone feels valued.
  • Competitive Benefits: Enjoy competitive salaries, performance-based bonuses, equity incentives, generous vacation, paid wellness days, and professional development support.

Hybrid and Remote Opportunities:
We offer flexible work arrangements, including hybrid and remote options tailored to individual roles.


Telix Pharmaceuticals is an equal opportunity employer. We evaluate candidates without regard to race, religion, gender, sexual orientation, disability, veteran status, or other legally protected characteristics.

For more details about our privacy policy, please click here.


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