Job details

Clinical Imaging Director

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.

VIEW OUR PRIVACY POLICY HERE

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$175000 / YEARLY (est.)

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What You Should Know About Clinical Imaging Director, Telix Pharmaceuticals (Americas)

Join Telix Pharmaceuticals as a Clinical Imaging Director and play a vital role in the groundbreaking field of radiopharmaceuticals! We're a rapidly expanding company committed to precision medicine aimed at improving the lives of those battling cancer and rare diseases. In this remote role, you’ll be at the helm of developing and executing advanced imaging protocols that are crucial to our research and clinical trials. Collaborating with a skilled team that includes Global Clinical Leads and Biostatistics experts, you'll leverage your expertise to optimize imaging data for innovative diagnostic and therapeutic radiopharmaceuticals. Your leadership will steer the creation of clinical study documentation and regulatory submissions, ensuring all imaging data is accurate and meticulously overseen. With a focus on oncology, you will engage with both investigators and vendors, maintaining the highest standards of compliance and quality control in your work. Your contributions will be crucial as we advance our approved prostate cancer imaging agent and tap into the immense potential of our late clinical-stage products. At Telix, we appreciate creativity and collaboration, and you’ll be part of a supportive global team that values diversity and innovation. We offer competitive salaries, annual bonuses, equity programs, and generous leave policies to promote your well-being and professional growth. If you are experienced, results-oriented, and driven by a purpose to make a difference in the oncology space, then consider bringing your talents to Telix Pharmaceuticals!

Frequently Asked Questions (FAQs) for Clinical Imaging Director Role at Telix Pharmaceuticals (Americas)

What are the key responsibilities of a Clinical Imaging Director at Telix Pharmaceuticals?

As a Clinical Imaging Director at Telix Pharmaceuticals, your main responsibilities include developing and executing imaging protocols for oncology clinical trials, overseeing the quality control of imaging data, and collaborating closely with cross-functional teams. You will also be tasked with leading the imaging sections of study documentation and engaging with third-party vendors to ensure compliance with regulatory standards.