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
The Vice President, Clinical Science is a senior leadership role that exists within Telix to support the design, strategy, and operationalization of clinical trials during the drug development process from Phase 0 to Phase 4 clinical trials through the leadership over a team of subject matter experts (SMEs) consisting of clinical medical physics, clinical pharmacology, imaging sciences and biostatistics. Functioning as an expert facilitator to asset matrix teams, clinical science leads, and other internal stakeholders, this position will also lead and advise other parts of the organization through a formal consultation process. The position is required to ensure that the quality and the reliability of studies are maintained and that clinical trials meet their objectives in collaboration with other members of the clinical research team including Clinical Operations, Pharmacovigilance (PV), Medical Affairs, Regulatory, Quality, Manufacturing, R&D, and Business Development.
Key Accountabilities
Develop study documentation including, but not limited to study protocols, investigators brochures (IBs), informed consent documents, clinical dossiers for regulatory submissions
Provide scientific input into documentation including IBs, IMPDs, DSURs and CSRs
Review study data including safety and efficacy data for accuracy and quality
Triage and delegate work requests to the in-house team of SMEs, while providing timeline, resource and workload balancing
Work closely with Clinical Operations, Medical Affairs, and asset matrix teams to ensure compliance with organizational SOPs
Assist in development and participate as needed, in Steering Committees and Advisory Boards with global thought leaders in appropriate indications
Provide senior management personnel regular updates on the progress of the clinical research
Review imaging studies, and be qualified to provide input on interpretation, quality assurance, accuracy of imaging interpretation, and final review of imaging, protocols, and imaging charters prior to implementation
Coordinate efforts associated with clinical imaging, pharmacology, biostatistics, and physics SMEs to address complex trial related questions/strategy
Education and Experience
Scientific background with university degree and MD required
10+ years Clinical experience with strong sponsor or CRO experience required
5+ years’ experience leading teams required
Detailed knowledge of global clinical trial regulations
Formal training in clinical diagnostic imaging (e.g. Radiology, Nuclear Medicine, Radiation Oncology) with Clinical Fellowship level training in Oncology associated field
Familiarity with managing groups within matrix teams
Personal Attributes
Ability to plan, create, strategize and drive execution of multiple projects under tight timelines
Very good attention to detail and project completer
Ability to prioritize and manage time effectively
Strong organizational and interpersonal skills
Demonstrated proficiency in Microsoft Office (including Outlook, Word, PowerPoint, Excel)
Excellent oral and written communication skills
Ability to manage teams through complex problems and issues
Able to modulate and communicate with multiple stakeholders (e.g. Clinical Science, Managers, Physicists, Medical Affairs, Sales and Marketing etc.)
Authorities
Financial: In line with Delegations of Authority Policy of the Board
Key Capabilities
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
Strong autonomy and ability to learn quickly and independently.
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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