Clinical Supply Chain Coordinator - Clinical Trials
AstraZenecaPoland - warsawUpdate time: September 9,2021
Job Description

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 Chain Coordinator is the Supply Chain entry level role supporting the Global Clinical Supply Chain team to ensure the delivery of Clinical material and associated information to meet the agreed Clinical demand.

The CSCC supports GCSC team with task based activities that include:

  • Task activities related to manufacturing of drug substance, drug product and packaged supplies including:
    • Management of drug packing activities;

    • Review of documentation related to drug packing jobs;

    • IRT system (IxRS) management;
    • Support in drug release activities.
  • Management of Documentation pertaining to SCM activities including:
    • Electronic Trial Master File documentation upload;
    • Invoice checking;
    • Archiving.
  • Ensuring continuous supply of Clinical Material to patients by completing the following activities:
    • Temperature Control Monitor tracking;
    • Complaints management;
    • Drug demand prediction activities as instructed by Clinical Supply Study Leader.

Education, Qualifications, Skills and Experience:

Essential:

  • University degree
  • Knowledge of R&D supply chain and drug development process.
  • Knowledge of Clinical Development processes relevant to investigational products.

Desirable:

  • Working knowledge of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products.

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!

Date Posted

08-wrz-2021

Closing Date

15-paź-2021

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 authorization and employment eligibility verification requirements.

Get email alerts for the latest"Clinical Supply Chain Coordinator - Clinical Trials jobs in Poland - warsaw"