Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.
See Yourself at Telix
We are seeking an experienced Oncology Clinical Imaging expert to join the Nuclear Medicine Center of Excellence (NMCOE) for Telix Pharmaceuticals, under the Division of Precision Medicine. The successful candidate will be responsible for design and execution of imaging protocols using standard and advanced radiological techniques. Optimizing, analyzing and interpreting data from these studies to advance the development of novel diagnostic and therapeutic radiopharmaceuticals in the setting of cross functional teams will be required.
The Clinical Imaging Director will work closely with the respective Global Clinical Leads, Global Program Leads, Clinical Operations, Biostatistics and other relevant areas within the organization to advance Telix Group’s assets towards optimized clinical adoption. This will be undertaken via a deep knowledge of advances in imaging in oncology. Core team members of the NMCOE will include the successful candidate, a Nuclear Medicine Physician and Radiation Physicist.
Key Accountabilities:
- Develop/execute protocols and workflows on imaging studies to enable the advancement of diagnostic and therapeutic radiopharmaceuticals
- Lead development of imaging sections of clinical study documentation and regulatory documents
- Lead the design, analysis, review, and quality control of imaging data to ensure accuracy and quality
- Oversight of third-party vendors, such as imaging CROs
- Collaborate with Global Clinical Leads, Global Program Leads, Biostatistics, Clinical Operations, and other cross-functional colleagues to ensure strategic and effective implementation of novel imaging approaches in clinical studies
- Prepare and deliver presentations, proposals, and reports for senior management, partners, and other stakeholders
- Scientific input and oversight on studies with endpoints utilizing NM/SPECT/PET techniques
- Engage with investigators and visit sites
- Maintain compliance with regulations, ICH/GCP Guidelines.
- Image analysis/review sessions with study teams, sites and KOLs
- Input into AI/ML imaging initiatives
- Provide input to Business Development, M&A activity and Medical Affairs
Education and Experience:
- Bachelor’s degree in biomedical science or imaging-related field is required
- 10+ years of experience in nuclear medicine with a focus to oncology
- Experience in clinical development within the pharmaceutical or biotechnology industry
- Strong knowledge of clinical trial design, methodology, and regulatory requirements
- Track record of working effectively with imaging CROs and vendor management
- Experience in authoring clinical study and regulatory documents
- Familiarity with GxP and regulatory guidelines for clinical trials
- Experience in the use of image analysis software in radiology and nuclear medicine
Key Capabilities:
- Willingness to travel domestically and internationally, as needed
- Strong understanding of the nuclear imaging and therapy market, products, and technologies
- Excellent negotiation, communication, and interpersonal skills, with the ability to build and maintain relationships with diverse stakeholders
- Self-motivated, goal-oriented, and able to work independently as well as collaboratively within cross-functional teams
- Highly organized and able to prioritize deliverables across clinical assets/programs
- Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
- Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
- Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
- Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
- Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
- Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
- Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills
At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.
Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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