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22 часа назад

Senior Set-Up Coordinator (AI)

Формат работы
remote (только United_kingdom)/hybrid/onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Set-Up Coordinator (AI/CTMS): Managing the end-to-end design and implementation of protocol amendments, sponsor-driven changes, laboratory databases, and study set-up activities with an accent on clinical trial management systems, regulatory alignment, and data quality. Focus on applying AI-enabled tools, automation, and data analytics while coordinating sponsor deliverables and improving laboratory study execution across the full lifecycle.

Location: Livingston, West Lothian, United Kingdom; home-based, office-based, and hybrid options available

Company

hirify.global provides drug discovery, clinical development laboratory, biomarker, and healthcare intelligence services across global life sciences programs.

What you will do

  • Manage the end-to-end design and implementation of protocol amendments and sponsor-driven changes.
  • Design, configure, and validate laboratory databases and study set-up activities using CTMS and related digital platforms.
  • Plan and deliver laboratory project set-up and execution activities across the full study lifecycle.
  • Maintain ownership of amendment delivery, sponsor deliverables, and database quality.
  • Communicate with sponsors and CROs, providing input on technology-enabled study design and delivery.
  • Identify opportunities to improve efficiency and ways of working through AI, automation, data analytics, and digital transformation.

Requirements

  • Bachelor's degree in life sciences or a related field.
  • At least 1 year of relevant experience, preferably in the clinical, medical, or healthcare industry, or an equivalent combination of education, training, and experience.
  • Experience or demonstrated interest in AI, automation, data analytics, or digital transformation in clinical or laboratory environments.
  • Strong working knowledge of Clinical Trial Management Systems and laboratory data systems.
  • Ability to adapt quickly to new technologies and work in fast-paced, evolving environments.
  • Curiosity, proactivity, and motivation to explore emerging technologies and innovative solutions.

Culture & Benefits

  • Global exposure across diverse regions and regulatory frameworks.
  • Variety of therapeutic areas.
  • Collaborative and supportive team environment.
  • Access to cutting-edge, in-house technology.
  • Career development and progression opportunities.

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