10 дней назад
Clinical Supply Specialist
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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