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10 дней назад

Clinical Supply Specialist

Формат работы
remote (только Italy)/hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Italy
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
Clinical Supply Specialist (Clinical Trials): Supporting day-to-day clinical supply execution across EU and US studies with an accent on supply planning, IRT/RTSM operations, GMP, distribution, and shipment oversight. Focus on coordinating temperature-controlled logistics, monitoring inventory and expiry, resolving shipment issues, and managing vendor and stakeholder communication.

Location: Milan; remote or hybrid work acceptable, with occasional travel potentially required

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Support clinical study supply planning, demand and supply forecasting, resupply parameters, scenario planning, and risk mitigation.
  • Coordinate IRT/RTSM requirements gathering, vendor setup, user acceptance testing, change management, and ongoing maintenance.
  • Execute and oversee depot-to-site and site-to-site shipments across the EU and US, including temperature-controlled logistics when required.
  • Track shipments, resolve issues, and maintain related documentation.
  • Monitor inventory, expiry and lot management, reconciliation, and regular KPI and status reporting.
  • Collaborate with depots, couriers, packaging and labeling partners, IRT providers, internal stakeholders, and external vendors.

Requirements

  • Bachelor’s degree.
  • Proven experience in clinical trial supply operations across Phase I, II, and III multi-country studies.
  • Strong familiarity with GMP and IRT/RTSM workflows, including setup support, UAT, change controls, releases, and ongoing operations.
  • Understanding of global distribution and logistics across the EU and US, import/export basics, temperature excursions, and deviation handling.
  • Strong organization, prioritization, problem-solving, and stakeholder communication skills.
  • Fluent English required; additional languages are an advantage.

Culture & Benefits

  • Work directly with a single pharmaceutical sponsor while receiving the support and career opportunities of a global CRO.
  • Client-facing role with independent work and close collaboration with client counterparts.
  • Professional development, continuous training, and a supportive culture.
  • Global environment with more than 4,000 professionals across over 20 countries.
  • Equal opportunity workplace focused on diversity and inclusion.

Hiring process

  • CV submission is followed by an application acknowledgement.
  • Qualified candidates are invited to a phone interview as the first selection step.

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