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Manager, Clinical Supply Chain

Role overview

Qualifications

  • Bachelor's degree in Business, supply chain or related field or 8+ years of radiopharma experience
  • Experience in inventory management, packaging, labeling, and distribution in highly regulated industry
  • Strong communication skills

Responsibilities

  • Oversee and manage end-to-end supply chain activities related to clinical trials
  • Collaborate with cross-functional teams to ensure timely and accurate placement and delivery of clinical supplies
  • Proactively identify and mitigate potential supply chain risks
  • Track and analyze key supply chain metrics and provide recommendations for process improvements

Key facts

  • Remote from: United States
  • Full time
  • Senior (5-10 years)
  • English

Other skills

  • Packaging And Labeling
  • Communication
  • Collaboration
  • Resilience
  • Adaptability
  • Creativity
  • Results Focused
  • Ethical Standards And Conduct

About the company

ARTMS logo

ARTMS

Medical Devices & Equipment

ARTMS specializes in the physics, chemistry and materials science of cyclotron-produced radionuclides. Our core technology platform, the QUANTM Irradiation System™ (QIS™), is a complete cyclotron-based isotope production system designed to support high efficiency, large-scale and cost-effective production of commercially important medical isotopes such as zirconium-89 (89Zr), gallium-68 (68Ga), technetium‐99m (99mTc) and copper-64 (64Cu). QIS™ is used today by many of the major manufacturing networks to optimize production of a range of medical radioisotopes. ARTMS has been acquired by Telix Pharmaceuticals. Interested in joining the team? Search our open positions: https://telixpharma.com/careers/find-a-job/

Company details

IndustryMedical Devices & Equipment
Company size11 - 50

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Job description

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 Manager, Clinical Supply Chain is responsible for overseeing and managing the end-to-end supply chain activities related to clinical trials, clinical dose ordering, 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:

  • 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 order placement and delivery of clinical supplies.
  • Collaborate with logistics team to identify lane mapping for clinical study sites in new regions.
  • Organize clinical mock shipments to any new regions as required by program/study.
  • Review and analyze clinical dose orders and status’ on a regular basis, capturing any impact notes to the dose as required.
  • Coordinate implementation of investigational product labeling with approved label provided by Telix GRA, assist with 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.
  • Develops program models, contributes to the study specifications for studies, and provides investigational medicinal
  • product management for highly complex studies.
  • Contribute to creation of product and study specific IMP Handling manuals with Clinical Operations team.
  • Track and analyze key supply chain metrics and performance indicators, providing regular reports and recommendations for process improvements and cost optimization.
  • Stay up to date on 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:

  • Bachelors degree in Business, supply chain or related field or 8+ years of radiopharma experience.
  • Inventory management, packaging, labeling, and distribution experience in pharmaceuticals or highly regulated industry a plus.
  • Coordinate and share investigational product labeling with CMO for each clinical product and region-specific label approved by GRA, assist with packaging sourcing if needed, and distribution activities, ensuring compliance with regulatoryguidelines 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.
  • Track and analyze key supply chain metrics and performance indicators, providing regular reports and recommendations for process improvements and cost optimization.
  • Stay updated on industry best practices, trends, and emerging technologies in clinical supply chain management, andincorporate relevant advancements into the company’s supply chain strategies and operations.

 

Key Capabilities:

  • 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
  • Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to 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
  • Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
  • Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
  • Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
  • 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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Marcus Rivera

Chief Revenue Officer

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