Clinical Supply Chain Professional
il y a 2 semaines
PSI CRO is an award-winning full-service Contract Research Organization (CRO) that brings together over 2,700 dynamic and knowledgeable individuals working to impact the future of medicine in more than 60 countries worldwide. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials of new medicines. Our work helps patients in need improve their well-being – a fundamental driver for many of us to show up and do our best each day.
Key Responsibilities- Analyze clinical trial protocols and translate requirements to establish an efficient supply chain solution for PSI studies.
- Build and maintain a drug demand forecast in line with planned enrolments.
- Plan the optimal campaign strategy to ensure clinical supplies are available in accordance with the project requirements.
- Manage the CMO vendor - oversee packaging, labelling, procurement, distribution and QP release activities to ensure supplies are delivered on time.
- Manage the IRT vendor - lead study-specific system set-up, UAT, system acceptance, and ongoing system updates.
- Develop clinical supply plans and provide input for the development of vendor management plans.
- Participate in the selection of trial supply vendors and IRT vendors for PSI studies.
- Support and train PSI teams in clinical supply management.
- Liaise with PSI project teams, company divisions, clients, and vendors.
- Assess risks associated with clinical product management and quality incidents reported by vendors.
- Support business development tasks related to clinical trial supply services.
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