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UCB

Associate Director, Clinical Trial Devices (United Kingdom)

Hybrid • Brussels, BEL, United Kingdom • Unknown • Не указана
Зарплата
Не указана
Опубликовано
13 ч назад
Описание

Make your mark for patients

We are looking for an Associate Director, Clinical Trial Devices to join us in our Global Regulatory Device Strategy team, based in our office in Belgium, Brussels.

About The Role

The Associate Director, Clinical Trial Devices (Device Single Point of Contact, DSPOC) is accountable for end-to-end leadership, coordination, and oversight of all device-related activities across the clinical lifecycle of assigned candidates and assets in clinical drug development. This includes in vitro diagnostics (IVDs), investigational medicinal product preparation and administration devices (IMPPADs), digital health technologies (DHTs), and other off-the-shelf medical devices.

Who You’ll Work With

This role connects clinical drug development with the device landscape. As an integral member of clinical teams, the DSPOC brings together device SMEs, backbone functions, and external partners to ensure clear ownership, alignment, and traceability of device-related activities and decisions.

What You’ll Do

  • Lead the DICE (DevICEs across the clinical lifecycle) end-to-end device process at the candidate/asset and study levels, ensuring effective planning, execution, coordination, and oversight across all stages.
  • Define and drive the device strategy by anticipating needs early, enabling proactive, risk-based decision-making, and ensuring full integration into clinical drug development, study design, and study documentation.
  • Support the selection of fit-for-purpose devices aligned with study endpoints, target population, and operational context.
  • Lead the creation, approval, and maintenance of key deliverables, including the Device Strategy Document (DSD), Device Study File (DSF), and Device Assessment Report Document (DARD).
  • Serve as the accountable person for all device-related activities, decisions, ...

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