VP, Global Clinical Operations

at  Telix Pharmaceuticals EMEA

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.

EDUCATION:

• Bachelor’s degree in a Medical, Science, Pharmacology or relevant related field is required
• Master’s degree or higher in a science and business field (e.g. MBA and PhD) is preferred.

EXPERIENCE:

• 15+ years’ experience in Clinical Operations / Clinical Development within a pharmaceutical or biotechnology environment is required.
• Experience within oncology and/or nuclear medicine is required.
• Previous experience in progressively higher responsibility roles within Clinical Operations, such as Director of Clinical Operations or equivalent is required.
• Extensive experience in managing and leading teams, including experience in a leadership role within Clinical Operations.
• Strong knowledge and understanding of region-relevant clinical trial regulations, guidelines, and industry standards, including GCP and applicable local regulations.
• Proven track record of successfully leading the execution of clinical trials (Phase I-IV), generating and compiling the clinical components of a regulatory submission, managing multiple programs, and ensuring adherence to timelines, budgets, and quality expectations.
• Expert in working with cross-functional teams and collaborating with other functions such as regulatory affairs, medical affairs, finance and research and development.
• Broad experience with the development and implementation of clinical operational strategies, processes, and best practices.
• Broad experience in risk management, compliance, and quality assurance within clinical operations.
• Demonstrated ability to drive innovation, process improvement, and operational efficiencies within clinical trial execution.
• Experience of interacting with regulatory agencies in preparation for, and during clinical audits.
• 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.
• Willingness to travel domestically and internationally, as needed.
  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.

Please refer the Job description for details