6 дней назад
Clinical Supply Chain Manager (Clinical Trials)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Supply Chain Manager (Clinical Trials): Developing and managing end-to-end supply strategies for clinical trials with an accent on protocol interpretation, kit design, forecasting, packaging, distribution, and regulatory compliance. Focus on coordinating vendors, managing IRT inventory, assessing temperature excursions, tracking budgets, and mitigating supply chain risks.
Location: Reading, Berkshire, United Kingdom; full-time, onsite role. Not eligible for UK visa sponsorship.
Company
Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Interpret clinical trial protocols and develop end-to-end clinical supply chain solutions.
- Create master English label text, demand forecasts, packaging plans, distribution plans, and temperature excursion management plans.
- Initiate packaging campaigns and oversee vendors to ensure on-time delivery of clinical supplies.
- Set up, monitor, and update Interactive Response Technology systems to manage study inventory.
- Track project budgets, conduct risk assessments, and implement appropriate mitigations.
- Lead client and vendor meetings and maintain compliance with GxP, regulatory, and training requirements.
Requirements
- Bachelor's degree in a science or business discipline preferred but not essential.
- 3–5 years of industry experience in clinical trials.
- 3–5 years of experience in clinical supply chain management.
- Demonstrated project management, communication, stakeholder relationship, direction, and problem-solving skills.
- Strong Microsoft Office skills, including Word, Excel, and PowerPoint.
- Proficiency in English is required.
Culture & Benefits
- Full-time position supporting clinical research and the development of medical treatments.
- Collaboration with internal teams, clients, and external vendors.
- Work focused on high quality standards, study timelines, regulatory compliance, and patient outcomes.
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