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Technical Start-Up and Delivery Director - Evinova

AstraZeneca
US, United States, United StatesRemotefull_timeVerifiedPosted 28 May 2025
💰 $214,111/yr($142,741/yr$214,111/yr)

About the role

Job Title: Technical Start-Up and Delivery Director
Location: Field Based (US East Coast Preferred)

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. 

This is a remote position for candidates on the US East Coast as a first preference, but also open to candidates based in Europe. We're seeking an independent problem solver with a collaborative spirit, eager to engage with team members around the globe. Join us and be part of a dynamic environment that values curiosity and teamwork!  

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 global health tech business might be for you!  

Transform 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. 

Introduction to Role:

This role is central to Evinova’s success. We are establishing the teams, processes, and capabilities needed to ensure seamless configuration, validation, and sustained support of our products across global clinical trials. Our goal is to deliver reliable, compliant, and high-quality technical solutions that bring study protocols to life through a consistent, patient-centric digital experience.

You will play a pivotal role in shaping how our product is brought to life for each study. Working in close partnership with Commercial, Delivery, Product, and Clinical teams, you will ensure our products are accurately configured, thoroughly tested, and continuously supported throughout the study lifecycle. Your leadership will drive operational excellence, regulatory compliance, and trusted delivery, differentiating Evinova through quality and service.

Accountabilities:

This is a high-impact role; the teams you lead directly impact patient experience and you can shape how Evinova delivers its digital clinical trial solutions to sponsors and studies. 

  • Study Implementation & Configuration:  You’ll lead teams responsible for translating complex clinical protocols and sponsor requirements into platform configurations, ensuring timely and accurate deployment. You’ll establish scalable, repeatable processes that enable rapid study start-up while maintaining the highest standards of compliance and quality.
  • Ongoing Maintenance & Technical Support: Beyond initial implementation, you’ll ensure each study continues to run smoothly throughout its lifecycle. This includes owning the processes for technical maintenance, issue resolution, and updates or reconfigurations. You’ll build frameworks to support long-term study success, reducing cost, downtime and enhancing user satisfaction across patients, sites, and sponsors.
  • Team Leadership & Capability Building:  You’ll build and lead high-performing technical delivery teams, fostering a culture of ownership, learning, and continuous improvement. You’ll set clear expectations, provide mentorship and direction, and create pathways for growth as the team scales with the business. You’ll also define best practices for delivery, configuration, and study validation across the team.
  • Cross-Functional Collaboration: You’ll work closely with Product, Engineering, Clinical, and Delivery teams to ensure study-specific configurations are feasible, efficient, and aligned with the platform’s technical capabilities. While you won’t own the core product roadmap, you’ll provide critical input based on real-world delivery experience and operational feedback.
  • Regulatory Compliance & Validation: Operating in a GxP and SaMD-regulated environment, you’ll ensure that all study configurations, testing activities, and documentation meet relevant quality and regulatory standards

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Company

AstraZeneca

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