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Global Study Planner Breda SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • HBO of hoger
  • Medior/Senior
  • Engels (taal)

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  • Vast contract
 

Vacature in het kort

Breda
Join a renowned biotechnology company as a Sr. Associate Global Study Planner, where you will independently manage global demand and supply planning for clinical studies. Your role will involve coordinating packaging, labeling, and inventory management, ensuring timely drug supply from study initiation to closure. Engage with cross-functional teams to support clinical trial success. Enjoy unique opportunities to participate in global meetings and enhance your expertise in a dynamic environment. Uncover the reasons why this position could elevate your career.
 

Over het bedrijf

SIRE Life Sciences
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The Company
This renowned biotechnology company specializes in developing the newest pharmaceuticals. With numerous facilities spanning across the globe, the company's primary focus is leveraging scientific research to create a positive impact on both humanity and the world. The Dutch facility plays a big part in the distribution part of the company.

Role Description
As a Sr. Associate Global Study Planner at this company, you will independently manage global demand and supply planning for clinical studies, ensuring timely and efficient drug supply from study initiation to closure. You’ll coordinate packaging, labeling, and inventory management while actively engaging with cross-functional teams to support clinical trial success.

Responsibilities
-Independently execute demand and supply planning for assigned global clinical studies (typically fewer than 10).
-Ensure timely supply of Finished Drug Product (FDP) from study start through to study closure.
-Manage packaging and labeling orders based on current study demand forecasts.
-Ensure supply readiness for new studies and monitor ongoing study inventory levels.
-Balance inventory levels with scrap risk and corporate inventory guidance.
-Resolve logistical issues that may impact study timelines or R&D milestones.
-Identify and escalate supply-related risks to stakeholders and internal management.
-Participate in and lead forecast meetings with global study managers (UK/US).
-Coordinate drug distribution to central warehouses and clinical sites.
-Maintain and update planning systems such as SAP, Forecasting tools, and internal dashboards.

Requirements
-Bachelor’s degree or equivalent in Logistics, Business Administration, or a related field
-Minimum 5 years of relevant experience in supply planning, preferably within the pharmaceutical industry
-Fluency in English, both written and verbal
-Knowledge of clinical supply chain management
-Experience using ERP systems, preferably SAP
-Strong communication and stakeholder management skills

Other information
Apply to our vacancy below for more information. looking forward to hearing from you!
 

54835

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