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Clinical Supply Coordinator 12 Month Contract

Astra Zeneca
Job LocationMacclesfield
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract, full-time

Job Description

Clinical Supply Coordinator - 12 Month Secondment / Fixed Term Contract / Fixed Term Opportunity Location: UK (Macclesfield)At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.The Clinical Supply Coordinator (CSC) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. What youll do The CSC supports GCSC teams with task-based activities that include performing tasks related to manufacturing of drug substance, drug product and packaged supplies including:

  • API order form creation
  • Bulk Drug order form creation
  • Packing Order Creation
  • Links Reports
  • Pre and post batch record review and release for primary and secondary packing jobs
  • IRT Upload
  • Release activities, such as T cards
    • Management of documentation activities including:
  • ANGEL documentation uploading
  • Electronic Trial Master File documentation archiving
  • Supporting RFQ updates with systems data
  • Invoice checking
  • Archiving
    • Ensuring continuous supply of clinical material to patients by performing the following activities:
  • Temperature Control Monitor tracking
  • Complaints management
  • Smart Supplies activities as instructed
  • Raise and track shipment requests - manual and IRT
  • Tracking activities as requested by SCM
    • Utilise SCM systems to support SCM activities:
  • IRT system
  • CARA
  • S-Life
  • SSF
  • LRA
    • This role covers parts of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products.In this role you will have the opportunity to work with multiple customers and partners internally and externally. You will follow SHE and GMP standards, and will be personally accountable for these areas within your own work Plans. Essential Requirements
  • Knowledge of Clinical Manufacturing & Supply and the drug development process
  • Knowledge of the Clinical Development processes relevant to investigational products
    • Desirable Requirements
  • Working knowledge of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products
    • At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested Come and join our journey. So, what’s next! Are you already imagining yourself joining our team Good, because we can’t wait to hear from you.AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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