Project Manager Clinical Supply Chain (33137)

Job description

Orion Group Life Sciences are looking for a Project Manager Clinical Supply Chain for our Multinational Pharmaceutical/Biotechnology client based in Breda. Initial 12-month contract, with a high possibility of extension. This is a hybrid position, where you have to be more onsite during initial training (minimal 3 days) and afterwards 50/50 onsite and remote.

Main Responsibilities of the role

• Develop and employ project management techniques to design and set up supply chains for clinical studies. This includes.
  • Create and maintain project plan to ensure timely clinical study start to support first subject enrolled per country cluster/ depot.
  • Create and maintain study forecast for finished drug product (both from our client and not from our client) in applicable systems to support clinical study start
  • Design optimal packaging configuration for finished drug product considering protocol requirements and product characteristics.
  • Ensure storage and shipping capabilities plus enough capacity for finished drug product is available within our clients supply chain network (both internal and external) to support global study footprint.
  • Design cost efficient (re)supply model to distribute finished drug product by considered risk analysis and mitigation strategy.
  • Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenarios, impact on study demand and set up activities for formulation and device introductions.

Required Qualifications and skills

• Knowledge of clinical supply chain management.
• Bachelors degree or equivalent in logistics, business administration or life science.
• Typically, 5 years relevant working experience, preferably in the Biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
• At minimum 3-year experience in project leadership and project management techniques in an international and regulated environment.
• General understanding of regulatory guidelines impacting clinical supplies (i.e., GxP, ICH guidelines, Clinical Trial Directive).
• Fluency in English, both verbal and written communication.
• Advanced experience in MS Office applications.
• Experience in using ERP systems, preferably SAP.
• Project Management certification (PMP, IPMA).

If you would like to have a confidential conversation regarding this opportunity please reach out to Tim Browaeys, tim.browaeys@orioneng.com or contact Tim on 0044 7593448607

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Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.