Label Specialist leads Label development projects/programmes. The individual has a working knowledge of project management methodologies, tools and templates and contributes to the development and maintenance of work products or change programmes. They ensure that business requirements are effectively captured and are responsible for effective tracking and reporting of project management information, as well as highlighting and supporting the resolution of areas of risk in project delivery.

 

 

The Global Clinical Supply Chain function is accountable for the supply of medicines to AstraZeneca’s clinical trials. In order to deliver medicine to patients in clinical trials the patient kits need to have translated and regulatory compliant label.

Label development is business-critical and linked to the overall delivery and approval of clinical trials. Frequently, label development activities are on the business-critical path for study set-up and start. 

 

There are key areas of Senior Label Specialist accountability/responsibility:

SME as a part of the Global Clinical Supply Chain organization, supporting label changes during study maintenanceInput into study setup/design strategy discussions to ensure the proper clinical labelling strategy is implementedLabel creationIdentifying cost saving, assessing timelines and implementing current label development process in optimal wayContinuous improvement of label development processes (SOPs, WI, GUI, training materials associated with label development)Involvement in system upgrades (initiating and driving improvements, review system options)Represent AZ as a part of broader Clinical Trial Sponsor’s community to collaborate in the field of new technologies implementation to the labelling process in general (includes external networks)Delivery of trainingsLeads and contribute to the team meetingsEnsuring effective stakeholders collaborationEscalation of risks/issues relating to the systems and activities through appropriate channelsDevelopment/input to key documents related label creationContribution to audits/inspections

 

The Label Specialist will require a deep and technical understanding of clinical trials, business processes, and the label technologies associated with clinical supply. Further key capabilities required for this role include:

Change enablement

Flexibility/adaptability

Works Collaboratively.

 

This role will impact the speed, quality, cost, and risk profile of development projects, affecting the availability of study drugs to patients.

 

Skills and Capabilities

Strong computing skillsExcellent English skills - verbal and writtenStrong communication skillsStakeholder managementTime and task managementPrioritisationProven analytical and strategic thinkingHigh attention to detailExcellent data management (entering, interpreting, analysing)Ability to learn new information effectivelyFlexibility to react to different customer needsGXP (i.e. GMP, GCP, GDP)

Date Posted

13-sie-2025

Closing Date

26-sie-2025

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.