Job Description

Job Title: Nonclinical Document SpecialistCareer Level - DIntroduction to Role:Are you ready to embrace new and varied opportunities to develop and learn? As a Nonclinical Document Specialist, youll work as a member of the Nonclinical Submission group with accountability for the technical quality and delivery of all nonclinical submissions. This is your chance to build nonclinical regulatory submissions for clinical trial and marketing applications in accordance with current standards and processes using agreed upon tools.Accountabilities:Your role will involve generating quality and nonclinical basic structures and content for regulatory submissions, ensuring relevant regulatory-authority compliant document naming conventions are applied to components. You will import and create documents for regulatory submissions including referenced literature and reference lists. Your responsibilities will also include submission document editing, submission readiness conformance with house-style, AstraZenecas submission ready standards and regulatory agency requirements. You will also contribute to the preparation and maintenance of submission document templates.Essential Skills/Experience:Expertise in using Document Management Systems gained in a pharmaceutical environment, eg, Veeva VaultExperience in understanding nonclinical dossier structures and advanced knowledge of common file formats (eg, Word) and related publishing tools (eg, ISI Toolbox, Adobe Acrobat, eCTDXPress)Knowledge of regulatory authorities requirements on electronic submissions in several regions (eg, US, Europe, etc.)Highly developed influencing skills and interactive communication when interacting with people at all levels and within teamsDemonstrated ability to set and manage priorities, resources, goals and project initiativesExperience working in cross-functional, global project teamsAwareness of basic principles of GXP and ICH (International Conference on Harmonization)Basic understanding of CTD (Common Technical Document) content and formatting standards to ensure submission compliant documentationProficiency in Microsoft Office and related suitesExperience working within validated electronic document management systemsFamiliarity with working within SharePointBasic knowledge of information management and document management tools and best practicesBachelors degree or equivalent industry-relevant experience3-5 years of industry experience in validated electronic document management systemsKnowledge of the basic principles of the drug development processBasic understanding of principles of CFR21 part 11 requirements and other global standardsExperience with Adobe Acrobat and related ISI tools (e.g. ISI toolbox)Experience as SharePoint site ownerWhen we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn\'t mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca, we are dedicated to following the science. Join the team at the heart of AstraZeneca that is committed and encouraged to follow the science. Driven by our curiosity, passion and determination we are paving the way to change the practice of medicine.Ready to make a difference? Apply now and join us in our mission.Date Posted 31-Jul-2024Closing DateAstraZeneca 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.

AstraZeneca