Назад
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4 часа назад

Associate Director, Clinical Operations

Формат работы
remote (только United_kingdom)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
UK/Ireland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Associate Director, Clinical Operations (Clinical Research): Planning and delivering global clinical development programs with an accent on clinical operations strategy, study execution, regulatory compliance, budgets, timelines, and risk management. Focus on overseeing study deliverables, aligning cross-functional stakeholders, managing vendors, and solving complex operational issues across clinical trials.

Location: Remote/home-based in the UK, with locations listed in Cambridge, Cambridgeshire, or London

Company

hirify.global is a global biopharmaceutical company developing medicines for serious diseases, with a focus on oncology, neuroscience, sleep disorders, and epilepsy.

What you will do

  • Provide clinical operations expertise for the planning and delivery of clinical development programs.
  • Define and operationalize program strategy with therapeutic and functional leadership.
  • Drive the development and alignment of protocols, clinical study reports, investigator brochures, and other clinical documents.
  • Oversee study team deliverables, enrollment, milestones, inspection readiness, timelines, budgets, and forecasts.
  • Support country feasibility, vendor selection, contracting, oversight, and risk mitigation.
  • Lead cross-functional improvement initiatives and mentor colleagues across clinical programs.

Requirements

  • Typically 10+ years of clinical research experience in the pharmaceutical or biotechnology industry, with deep clinical operations expertise.
  • Strong understanding of global clinical trial regulations, ICH/GCP guidelines, and regulatory compliance.
  • Experience interacting with functional leaders, major vendors, and senior leadership on program strategy and execution.
  • Financial acumen in managing clinical trial budgets, forecasting spend, and making cost-effective decisions.
  • Ability to collaborate cross-functionally, influence stakeholders, manage complex projects, and prioritize competing demands.
  • Bachelor of Science or Master of Science degree in a related discipline, or equivalent experience; an advanced degree is preferred.

Culture & Benefits

  • Remote/home-based working arrangement.
  • Opportunity to contribute to patient-focused, science-driven research and development.
  • Collaboration with Clinical Development, Data Management, Biostatistics, Regulatory, vendors, and other stakeholders.
  • Focus on operational excellence, continuous improvement, and adoption of new ways of working.

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