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Senior Clinical Supply Chain Manager

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Clinical Supply Chain Manager (Clinical Trials): Leading the planning, oversight, and delivery of clinical trial supply chain projects with an accent on demand forecasting, packaging, distribution, IRT systems, and regulatory compliance. Focus on managing temperature excursions, assessing operational risks, coordinating vendors, and ensuring clinical supplies reach the right place at the right time.

Location: London, United Kingdom

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead strategic planning, oversight, and delivery of clinical supply chain projects across global clinical studies.
  • Interpret clinical trial protocols and develop supply chain, demand forecasting, packaging, and distribution plans.
  • Create master English label text in line with applicable regulatory frameworks, including Annex 13.
  • Set up and monitor Interactive Response Technology systems to manage study inventory.
  • Coordinate packaging and distribution vendors, track budgets, and lead client and vendor status meetings.
  • Develop temperature excursion management plans, assess reported excursions, and implement risk mitigations.

Requirements

  • Bachelor’s degree in Life Sciences, Supply Chain Management, Business, or a related discipline.
  • At least 5 years of clinical supply chain management experience within the clinical trials industry.
  • Hands-on experience with Interactive Response Technology systems and clinical trial supply planning.
  • Project management skills with the ability to coordinate and deliver multiple priorities.
  • Strong stakeholder management, communication, interpersonal, problem-solving, and influencing skills.
  • Fluent English with excellent written and verbal communication skills. Proficiency in Microsoft Word, Excel, and PowerPoint is also required.

Culture & Benefits

  • Work within a global provider serving the life sciences and healthcare industries.
  • Contribute to continuous improvement and the optimisation of clinical trial supply processes, systems, and capabilities.
  • Maintain compliance with assigned training, GxP requirements, and applicable regulatory standards.
  • Participate in client bid defence meetings and support the ongoing development of the Clinical Trial Supplies department.

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