Introduction to role:

Are you ready to build a global trusted foundation of evidence that powers compliant content and accelerates approvals for life-changing medicines In this role you will create the single source of truth for references and core claims that enables our teams to move faster reduce rework and set the standard for quality across markets!

You will work at the intersection of science content and technology partnering with Medical Regulatory markets brands and agencies to make every claim traceable and every asset reusable. Apply if you see yourself designing a library where content creators and reviewers find what they need in seconds and where every decision is anchored to rock-solid evidence.

Accountabilities:

Establish and handle the worldwide repository of references and core claims in Veeva Vault PromoMats. This allows reuse and consistent governance across markets and brands.

Claims and Reference Ingestion: Orchestrate intake of core claims link them to supporting references and structure the library for searchability and Medical Legal and Regulatory (MLR) readiness.

Medical Partnership: Collaborate with Medical teams to validate accuracy appropriateness and currency of references so reviewers can approve with confidence and fewer cycles.

Metadata and Taxonomy: Define apply and implement tagging standards for references claims images illustrations and modular content to enhance findability and reporting.

Quality Control and Audits: QC new claims references and metadata; run periodic audits with Medical/Regulatory; update content as source materials evolve to maintain compliance.

DAM and Rights Management: Ensure complete image and illustration rights metadata in PromoMats and that all file components are included for compliant submissions.

User Enablement and Support: Provide multi-country user support training access management and troubleshooting to drive adoption and self-service retrieval.

Agency and Partner Engagement: Guide agencies on correct submissions claimreference linking and adherence to standards to reduce rework and speed approvals.

System Implementation: Contribute to user acceptance testing and rollout of content system enhancements; translate feedback into practical improvements.

Business Impact: Convert librarian rigor into measurable outcomeshigher reuse rates cleaner MLR submissions and faster time to approval that scales across markets.

Essential Skills/Experience:

• A bachelors degree or equivalent experience preferably in Life Sciences; a Library Science degree is preferred.
• A scientific background with familiarity with medical terminology and various types of medical references.
• Approximately 5-7 years of proven experience in maintaining a global library of references core claims and reusable assets ideally within Veeva Vault PromoMats.
• Strong knowledge of pharmaceutical referencing core claims management and content governance practices.
• Proficiency in Microsoft Office Suite Adobe Creative Suite and Veeva Vault PromoMats.
• A solid understanding of creative asset file types data classification frameworks and medical reference-to-claim linking.
• Strong communication stakeholder management planning prioritization and organizational skills.

Desirable Skills/Experience:

• Experience configuring Veeva Vault PromoMats object types lifecycles and metadata models.
• Hands-on digital asset management in regulated environments including rights management and reuse workflows.
• Direct involvement in MLR submission processes across multiple countries or brands.
• Experience delivering user training at scale and producing clear guidance and standards.
• Familiarity with taxonomy design controlled vocabularies and ontology management.
• Exposure to UAT planning test case design and defect triage for content systems.
• Ability to coordinate agencies and vendors and drive adherence to submission standards.
• Working knowledge of content data quality metrics and dashboarding.

Why AstraZeneca:

Join a high-performing digitally savvy team that partners across the enterprise to unlock the power of science for patients. Here we are evidence specialists creatives technologists and medical reviewers come together to turn ideas into real change - accelerating how we operate today while preparing for tomorrow. You will be trusted with relevant accountability listened to and empowered to focus on what truly moves the business. We adapt quickly and think enthusiastically. We support each other so you can stretch learn and build an outstanding reputation. You will also see the direct impact of your work on patients worldwide.

Call to Action:

Lead the evidence backbone that speeds compliant high-quality content to markettake the next step and help us set a new standard for claims and references at global scale.

Date Posted

Closing Date

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.