VP, Clinical Science

Role Summary

The Vice President, Clinical Science is a senior leadership role at Telix responsible for designing, strategy, and operationalizing clinical trials from Phase 0 through Phase 4. The role leads a team of subject matter experts in clinical medical physics, clinical pharmacology, imaging sciences, and biostatistics, serving as an expert facilitator to asset matrix teams and clinical science leads. The position ensures the quality and reliability of studies, guiding the organization through a formal consultation process with Clinical Operations, Pharmacovigilance, Medical Affairs, Regulatory, Quality, Manufacturing, R&D, and Business Development. It also supports the international rollout of Telix’s approved imaging agents and late-clinical-stage products addressing significant unmet needs in oncology and rare diseases.

Responsibilities

• 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

Qualifications

• 10+ years Clinical experience with strong sponsor or CRO experience
• 5+ years’ experience leading teams
• Detailed knowledge of global clinical trial regulations
• Familiarity with managing groups within matrix teams

Education

• Scientific background with university degree and MD required
• Formal training in clinical diagnostic imaging (e.g. Radiology, Nuclear Medicine, Radiation Oncology) with Clinical Fellowship level training in Oncology associated field

Skills

• 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.)