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Clinical Supply Chain Manager

2 months ago


Rockville, Maryland, United States Immunocore Limited Full time
Job Details:

Vacancy Name: Manager, Clinical Supply Chain
Vacancy No: VN447
Employment Type: Full Time
Location of role: Conshohocken, PA; Rockville, MD; Abingdon, UK
About Immunocore:

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company focused on developing transformative medicines addressing unmet patient needs in oncology, infectious diseases, and autoimmune diseases. We create an environment for collaboration and innovation while striving for a diverse and inclusive workplace.
Key Responsibilities:

  • Ensure effective management of drug manufacturing and the clinical supply chain.
  • Lead Supply Chain discussions in team meetings and communicate effectively with customers and partners.
  • Set up clinical supply chain strategy for studies.
  • Design and implement labelling, packaging, and supply strategies.
  • Manage the generation and approval of label texts and translations.
  • Produce clinical supply agreement documents.
  • Ensure supply chain strategy delivers clinical supplies effectively, balancing cost and risk.
  • Monitor budgets for individual study and program activities.
  • Manage relationships with vendors and oversee labelling, packaging, and distribution activities.
  • Ensure compliance with regulatory requirements for IMP and ancillary materials.
  • File clinical supplies documentation appropriately.
  • Support compliance with Immunocore's Quality Management system.
  • Present and train clinical trial personnel as necessary.
  • Assist with troubleshooting site clinical pharmacy issues.
  • Provide guidance to junior clinical supply chain personnel.
Requirements:
  • Significant experience in managing clinical trial supplies.
  • Project Management skills.
  • Experience in cold chain supply management and biopharmaceuticals.
  • Excellent attention to detail and strong interpersonal skills.
  • Thorough understanding of GxPs and global regulatory requirements.
  • Excellent organizational and computer skills.
Desirable:
  • Experience in all phases of clinical trials.
  • Knowledge in Oncology therapeutic discipline.
Education & Qualifications:
  • Degree or higher degree in a relevant scientific subject or business management.
  • Desirable: Masters or PhD in a relevant scientific subject.

Work authorization and a valid passport are required for this role. US applicants must be US Citizens/Permanent Residents.

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