Sr. Manager, Clinical Supply Chain

Posted:
10/28/2024, 4:14:09 AM

Experience Level(s):
Senior

Field(s):
Operations & Logistics

Workplace Type:
Hybrid

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 Senior Manager, Clinical Supply Chain is responsible for overseeing and managing the end-to-end supply chain activities related to clinical trials and the distribution of radiopharmaceutical products. You will collaborate closely with cross-functional teams, including Clinical Operations, Quality, Regulatory, Manufacturing, and Logistics, to ensure the efficient and timely delivery of clinical supplies while adhering to regulatory requirements and company standards.  

Key Accountabilities:

  • Develop and implement strategic plans and operational strategies for the clinical supply chain, ensuring alignment with the company’s overall objectives and goals. 
  • Oversee all aspects of clinical supply chain management, including demand forecasting, planning, sourcing, procurement, inventory management, packaging, labeling, and distribution. 
  • Collaborate with cross-functional teams to establish and maintain effective relations with clinical sites, CMOs, and third-party logistics providers, ensuring the timely and accurate delivery of clinical supplies. 
  • Partner with Clinical Operations and Manufacturing teams to define and manage clinical trial supply strategies, including drug forecasting, demand planning, and comparator sourcing. 
  • Coordinate and manage investigational product labeling, packaging, and distribution activities, ensuring compliance with regulatory guidelines and internal quality standards. 
  • Collaborate with Regulatory and Quality teams to ensure compliance with all relevant regulations, guidelines, and standards governing clinical supply chain operations. 
  • Proactively identify and mitigate potential supply chain risks and develop contingency plans to address any potential disruptions to the clinical supply chain. 
  • Independently responsible for conceptualization, development, and implementation of clinical supply plans, based on clinical study protocol and clinical development plans.  
  • Develops program models, contributes to the study specifications for IWRS studies, and provides medication management for highly complex studies using IWRS and predictive tools.   
  • Track and analyze key supply chain metrics and performance indicators, providing regular reports and recommendations for process improvements and cost optimization.
  • Stay abreast of industry best practices, trends, and emerging technologies in clinical supply chain management, and incorporate relevant advancements into the company’s supply chain strategies and operations. 

Education and Experience: 

  • Bachelor’s degree in relevant scientific or business discipline required
  • 8+ years’ experience in clinical supply chain management within the pharmaceutical, biotechnology, or radiopharmaceutical industry, with increasing levels of responsibility required
  • Strong understanding of clinical trial supply chain processes, including demand forecasting, planning, sourcing, and distribution. 
  • Excellent knowledge of relevant regulations, guidelines, and standards governing clinical supply chain operations, such as Good Manufacturing Practice (GMP), Good Clinical Practice (GCP) and Good Distribution Practice (GDP). 
  • Proficiency in utilizing supply chain management software systems and tools. 
  • Exceptional problem-solving and analytical skills, with the ability to make sound decisions in complex and time-sensitive situations. 
  • Strong communication and interpersonal skills, with the ability to collaborate effectively across functions and regions and influence key stakeholders. 
  • Detail-oriented mindset, with a focus on accuracy, quality, and compliance. 

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

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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