Senior Clinical Supply Manager (m/f/d)

​Professional | Permanent | Full-/ Part-time | Hybrid​

If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development , we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.

What the job looks like
Each day you'll enjoy a variety of challenges, such as:

• Being responsible for vendor relationship management and identifying potential external CTS service providers (e.g. Contract Manufacturing Organizations, Depots, Couriers, IRT providers)
• Being the central point of contact for all trial supplies related activities for all assigned trials/projects
• Developing trial-specific packaging concepts in alignment with relevant stakeholders to achieve packaging design which ensures a proper handling by site staff/patients and fulfils any blinding requirements
• Developing of trial-specific supply strategy including depot involvement to ensure in-time delivery of high quality clinical trial supplies
• Coordinating and overseeing of manufacturing tasks, e.g. planning, coordination of bulk manufacture, packaging and labelling, coordination of QP release, storage requirements
• Overseeing outsourced tasks related to any aspect of clinical trial supplies management to ensure adequate performance, implementation of risk management and issues are identified/communicated and corrective actions implemented and documented appropriately.
• Maintaining and delivering budget oversight and forecasts

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

• Pharmacist degree or comparable scientific, technical, or medical qualification
• >10 years-experience in Pharmaceutical Industry in field of Clinical Trial Supply Management, preferably CRO experience
• Experience in budget forecast and budget tracking
• Experienced in the conduct of clinical trials
• Thorough understanding of applicable EU and US GMP regulations for IMP manufacturing
• Thorough understanding of GDP requirements for setup of logistical part of supply chain and of GCP requirements in the conduct of Phase I – IV trials
• Excellent analytical, organizational and communication skills
• Service-oriented mindset whilst enjoying working in interdisciplinary teams

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