The Global Clinical Supply Chain function is accountable for the supply of medicines to AstraZeneca’s clinical trials. I order to deliver medicine to patients in clinical trials the patient kit need to have a translated and regulatory compliant label. The label development is business critical and linked to overall delivery and approval of clinical trials. Frequently the label development activities are on the business-critical path for study set-up and start.

Accountabilities / Responsibilities

The Label Specialist will perform and support wider Supply Chain organization via development of translated and regulatory compliant study labels using SmartSupplies LRA (Label Routing and Approval) module and LRA process. This includes activities related to new regulatory requirements for labels and identification of new base phrases in SmartSupplies LRA and overall label development process improvements. The Specialist must work according to label regulations (i.e. Annex 13) and Good Manufacturing Practice (GMP) standards.

The Supply Chain Label Specialist will act as expert and support/replace Clinical Study Supply Leads (CSSLs) in label development and change management: This will include:

• Help CSSLs convert supply chain study design in to label requirements
• Replace CSSL during translation activities with external vendor
• Author/review/approve Study Master label document/Label templates and label approval forms

In addition, as part of a wider Label Specialist Network, contribute to:

• Establishing best practice and ensure issues and learnings are shared both locally and globally
• Develop and continuously improve LRA processes, SOPs, procedures, and training materials associated with label development
• Perform updates to LRA database (country requirements and translations)
• Deliver Label training and guidance to CSSL groups
• Support wider Supply Chain organization with general label expertise

Education, Qualifications, Skills and Experience

The Global Clinical Supply Chain Label Specialist will require a deep and technical understanding of both the business processes and the label technologies associated with clinical supply.

Further key capabilities required for this role include: Change enablement; Flexibility/adaptability; Strategic leadership; Commitment to customers and integrity, and Works Collaboratively.

This role will impact the speed, quality, cost and risk profile of development projects and the overall portfolio and impact the availability of study drug to patients. As such, it has potential to significantly impact the financial and reputational dimensions of AstraZeneca.

Skills and Capabilities:

• University degree
• Strong computing skills
• Excellent English skills - verbally and written
• Proven analytical and strategic thinking
• Demonstration of high attention to detail
• Ability to learn new information effectively
• Flexibility to react to different customer needs
• Multi-language skills are a merit

Date Posted

17-cze-2021

Closing Date

10-lip-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.