CLINICAL CONTENT MANAGEMENT LEAD, EVINOVA

Are you ready to be part of the future of healthcare? Can you think big, be bold, and harness the power of digital and AI to tackle longstanding life sciences challenges?  Then Evinova, a new health tech business part of the AstraZeneca Group might be for you!      Transform billions of patients’ lives through technology, data, and innovative ways of working.
You’re disruptive, decisive, and transformative.
Someone excited to use technology to improve patients’ health.
We’re building a new Health-tech business – Evinova, a fully-owned subsidiary of AstraZeneca Group.
Evinova delivers market-leading digital health solutions that are science-based, evidence-led, and human experience-driven.
Thoughtful risks and quick decisions come together to accelerate innovation across the life sciences sector.
Be part of a diverse team that pushes the boundaries of science by digitally empowering a deeper understanding of the patients we’re helping.
Launch pioneering digital solutions that improve the patients’ experience and deliver better health outcomes.
Together, we have the opportunity to combine deep scientific expertise with digital and artificial intelligence to serve the wider healthcare community and create new standards across the sector.
About the Role   As the Clinical Content Management Lead, you will oversee and guide our growing team of Content Managers and Content Publishers who specialize in clinical trial content.
You'll play a key role in the deployment of our digital health products (web portals, mobile applications, and devices), ensuring high-quality study onboarding and meticulous management of sensitive clinical trial content across our solutions.
What You'll Do   In this role, you’ll.
Lead and Mentor.
Guide and mentor your team in managing clinical trial content, coordinating tasks, and ensuring high-quality delivery throughout the various stages of content management.
Be the Content Expert.
Serve as the primary point of contact for all internal stakeholders regarding study onboarding related to clinical content, aligning closely with project management, configuration, and product teams.
Collaborate.
Work closely with project management, configuration teams, and engineers, and lead content managers, and content editors to plan, assess, resource, reuse, store, process, and manage clinical trial content, including patient-facing screens, forms, translations, and study materials.
Streamline Clinical Processes.
Continuously improve and streamline the content management processes to enhance efficiency and quality.
Be the subject matter expert in all things content, as well as someone who is solution orientated.
Stakeholder Management.
Coordinate with internal and external partners, including clinical study teams and regulatory affairs, to ensure seamless execution of clinical content management tasks.
Advise on Content Creation and Management.
Lead content management activities for an assigned set of clinical studies, including advising on the design, creation, translation, localization, and publication of clinical trial content in the CMS, with the support of Content Publishers.
Quality Assurance.
Ensure an efficient and high-quality content management experience by continuously monitoring and improving clinical trial implementation and delivery.
S upporting submissions to regulatory and ethics committees.
A dhering to regulatory requirements and industry standards.
About You   You’re a natural leader with a strong background in content management within a highly regulated environment.
You have a deep understanding of the complexities and sensitivities involved in handling clinical trial data and materials.
You thrive in a collaborative, cross-functional setting and have a passion for improving healthcare through technology.
Specifically.
Are adaptable, able to pivot strategies in response to changing business needs.
Our products get better with every release.
Clinical protocols also change.
Love leading a team, collaborating with an international team of colleagues to find solutions to challenges, and making the process better after each project.
Have a focus on quality and ask team members questions to clarify requirements.
Be comfortable saying “no” and provide consultative solutions to design the best studies in Evinova’s software.
Minimum Experience   3-5 years ’ experience as a content manager in a regulated industry, with 1-2 years ’ experience as a team lead   Extensive hands-on experience as a Content Manager, ideally within the pharmaceutical, biotech, or healthcare industry, specifically managing clinical trial content.
H ands-on experience with digital /headless Content Management Systems (CMS) and a deep understanding of the content production lifecycle and content management strategy.
Proven leadership skills with experience managing and growing teams.
Excellent analytical, problem-solving, and communication skills with the ability to interact effectively with team members and stakeholder at all levels      Desirable Experience   Hands-on experience with Digital Asset Management systems (DAM).
Ideally an u nderstanding of regulatory requirements for clinical trial content management, including compliance with Good Clinical Practice (GCP) and data protection regulations.
Education in Life Sciences, Health Sciences, Biomedical Engineering, or a related field, or similar job experience.
Experience of working in a global organization with complex/geographical context    Background.
Content Stack, JIRA, Confluence, FIGMA, Miro, GitHub, Smartsheet, CMS,   eCOA, IVRS, RTSM, eConsent, Telehealth, EDC, GxP, Clinical Trials     Why Evinova (AstraZeneca)?   Evinova draws on AstraZeneca’s deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers.
Together, we can accelerate the delivery of life-changing medicines, improve the design and delivery of clinical trials for better patient experiences and outcomes, and think more holistically about patient care before, during, and after treatment.
We know that regulators, healthcare professionals, and care teams at clinical trial sites do not want a fragmented approach.
They do not want a future where every pharmaceutical company provides its own, different digital solutions.
They want solutions that work across the sector, simplify their workload, and benefit patients broadly.
By bringing our solutions to the wider healthcare community, we can help build more unified approaches to how we all develop and deploy digital technologies, better serving our teams, physicians, and ultimately patients.
Evinova represents a unique opportunity to deliver meaningful outcomes with digital and AI to serve the wider healthcare community and create new standards for the sector.
Join us on our journey of building a new kind of health tech business 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.
Learn more about Evinova www.
vinova.
om   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.