AstraZeneca

Clinical Supply Study Lead - Clinical Trials

1 day left

Location
Poland, Masovia, Warsaw
Salary
Negotiable
Posted
07 Jun 2021
Closes
14 Jun 2021
Ref
R-110409
Contact
AstraZeneca
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)


ABOUT ASTRAZENECA

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

SITE DESCRIPTION

Welcome to Warsaw Site, one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca's priorities, it's important to us that you bring your full self to work every day. To help you maintain your best self, here's a sneak peek into some of the things this site provides for you.

What you can expect: great working atmosphere empowering you to reach your full potential, endless development opportunities and benefits like: medical & life insurance, lunch card, annual bonus, education cost reimbursement, occasional allowances (Christmas, holiday), Multisport, anniversary awards, additional time off, pension plan, business travel insurance, recognition programme, flexible working hours.

At AstraZeneca, every one of our employees makes a difference to patient lives every day.

The Clinical Supply Study Lead (CSSL) designs and executes supply chain for one or more global clinical studies across all phases within drug development. The CSSL holds overall accountability for investigation of product and coordinates associated tasks and activities across all relevant functions within the supply chain. The role will have multiple contacts across internal and external groups including leadership of working groups.

There are key areas of CSSL accountability at the study level:

Study Design influence in relation to drug supply requirements Stakeholder management:

  • Lead the Study Drug Working Group and contribute to Supply Chain Team Meetings, to enable continuous cross-functional dialogue with the internal and external stakeholders on the study design requirements and their changes affecting supply chain of the study.
  • Lead/contribute to Kick Off Meetings for relevant suppliers (ie pack-label-distribution vendors, clinical CRO, IRT suppliers) and maintain collaboration throughout the study lifecycle
  • Escalation of risks / issues / concerns relating to systems and activities through appropriate channels

Demand and Supply - planning and management:

  • Development/input to key documents reflecting supply chain design & requirements
  • Refined initial and continuous study demand forecasting in order to create a Supply Plan for primary and secondary packing, together with identification of risks related to demand/supply
  • Inventory management

Cost management:

  • Assessment of projected costs related to packaging, labelling and distribution reflected in supplier Request for Quote
  • Control of ongoing study spend and invoice approval
  • Flagging risks related to budget constraints to the business

Compliance:

  • Management of Quality Events (ie Deviations, CAPAs, Complaints, Change Control)
  • Contribution to GMP & GCP audits
  • Ensuring eTMF compliance

System utilization:

  • IRT
  • System used for demand and supply planning
  • System used to optimize drug supply design

Packing/labelling/distribution activities:

  • Definition and implementation of pack/label/distribution strategy
  • Kit/Pack design
  • Implementation of Temperature Control and Monitoring strategy
  • Master Label development (if relevant)
  • Destruction management
  • Expiry date management
  • Extension of shelf life
  • Rework & recalls

Tasks related to the above areas can be supported where appropriate, by relevant Global Clinical Supply Chain supporting functions (Co-Ordinator or Specialists), however the CSSL retains overall accountability for delivery drug supply.

Why AstraZeneca?

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 cutting edge 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!

Where can I find out more?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/

Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en

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