Clinical Trials Supply Lead — Strategy & Delivery

ICON Clinical Research

Poland

A distancia

PLN 150.000 - 210.000

Jornada completa

14 días+

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Annual leave entitlements
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Employee Assistance Programme

Descripción de la vacante

ICON plc is seeking a Clinical Supplies Project Manager in Poland to design and analyze clinical trials, interpret complex data, and advance innovative treatments. You will oversee multi-workstream delivery, ensure regulatory-compliant supply management, and collaborate with cross-functional teams to optimize timelines and budgets.

The role emphasizes strong organizational, communication, and problem-solving skills, with a focus on stakeholder collaboration throughout project lifecycles.

Formación

  • Bachelor's degree in a relevant field such as pharmacy, life sciences, or supply chain management.
  • Proven experience in clinical supplies project management within pharma/biotech.
  • Strong understanding of regulatory requirements related to clinical trial supply management.
  • Excellent organizational and communication skills, with ability to guide cross-functional teams and drive project success.
  • Problem-solving mindset and adaptability to changing project dynamics.

Responsabilidades

  • Oversee planning and execution of clinical supplies projects ensuring timely delivery and regulatory compliance.
  • Collaborate with cross-functional teams to design and implement strategies for trial supply management.
  • Monitor and analyze project timelines, budgets, and resource allocations to optimize efficiency.
  • Address risks and challenges in clinical supplies logistics and implement solutions.
  • Foster relationships with internal and external stakeholders for effective lifecycle collaboration.

Conocimientos

Project management
Regulatory knowledge
Stakeholder communication
Problem solving
Cross-functional collaboration

Educación

Bachelor's degree in pharmacy, life sciences, or supply chain management

Descripción del empleo

ICON plc is seeking a Clinical Supplies Project Manager in Poland to design and analyze clinical trials, interpret complex data, and advance innovative treatments. You will oversee multi-workstream delivery, ensure regulatory-compliant supply management, and collaborate with cross-functional teams to optimize timelines and budgets.

The role emphasizes strong organizational, communication, and problem-solving skills, with a focus on stakeholder collaboration throughout project lifecycles.

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