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Global Category Manager – Clinical Jobs (Hybrid work)

3 Job Offers

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Global Category Manager – Clinical
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Join a leading global brand in Madrid as a Global Category Manager for Clinical Procurement. You will drive strategic sourcing and supplier management for clinical trials, CROs, and lab services. This role requires proven pharma R&D procurement experience and offers a chance to shape category str...
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Spain , Madrid
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55000.00 - 65000.00 GBP / Year
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Bramwith Consulting
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Until further notice
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Global Category Manager - Clinical / Direct Procurement
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Lead strategic procurement for clinical and R&D categories from our Munich hub. You will manage sourcing, vendor negotiations, and supplier performance across clinical trials, lab services, and equipment. This role requires proven pharma procurement expertise and offers a key position in a global...
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Germany , Munich
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55000.00 - 65000.00 GBP / Year
bramwithconsulting.co.uk Logo
Bramwith Consulting
Expiration Date
Until further notice
New
Global Category Manager - Clinical / Direct Procurement
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Lead strategic procurement for clinical and R&D categories from our Madrid hub. You will manage sourcing, vendor negotiations, and supplier performance in a regulated, science-led environment. This role requires proven experience in pharma/healthcare procurement and expertise with RFPs, MSAs, and...
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Location
Spain , Madrid
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Salary
55000.00 - 65000.00 GBP / Year
bramwithconsulting.co.uk Logo
Bramwith Consulting
Expiration Date
Until further notice
A Global Category Manager in Clinical jobs is a senior strategic procurement professional who acts as the architect of supply and partnership strategies for all goods and services related to clinical research and development within the pharmaceutical, biotechnology, and broader life sciences industries. This role is pivotal in ensuring that the complex, high-stakes process of bringing new drugs and therapies to market is supported by robust, compliant, and cost-effective external partnerships. Professionals in these jobs sit at the critical intersection of science, business, and compliance, managing multi-million dollar categories that directly impact R&D timelines, data integrity, and patient safety. The core responsibility of a Global Category Manager – Clinical is to develop and execute comprehensive category strategies for the external spend involved in clinical trials. This encompasses a wide range of specialized services and products, including full-service Clinical Research Organizations (CROs), central laboratory and diagnostic services, bioanalytical testing, clinical trial technology platforms, lab equipment and consumables, and patient recruitment services. Their work is far from merely transactional; it involves deep market analysis, supplier relationship management, and rigorous risk mitigation. They lead complex global sourcing events, such as RFPs and negotiations, to establish master service agreements and rate cards that deliver both significant commercial value and guaranteed service quality. A defining aspect of these jobs is the necessity for exceptional cross-functional collaboration. Category Managers work intimately with key internal stakeholders from Clinical Operations, Regulatory Affairs, Quality Assurance, Legal, Finance, and R&D scientific teams. They translate scientific and operational needs into clear procurement requirements, ensuring all contracts and partnerships adhere to stringent regulatory standards (like GxP) and audit readiness. They are also responsible for ongoing supplier performance management, using key performance indicators (KPIs) and benchmarks to ensure vendors deliver on time, within budget, and to the required scientific and compliance specifications. Typical skills and requirements for professionals seeking Global Category Manager – Clinical jobs include a proven background in strategic procurement within a highly regulated environment, preferably pharmaceuticals or biotech. Direct experience with clinical or R&D categories is essential. They must possess strong expertise in end-to-end sourcing processes, contract law fundamentals, and financial analysis. Crucial soft skills include superior stakeholder influence, strategic thinking, and a process-improvement mindset. Familiarity with procurement systems (e.g., SAP Ariba) and professional qualifications like CIPS are often advantageous. Ultimately, individuals in these jobs are critical enablers of innovation, building the external ecosystem that allows life sciences companies to conduct reliable, efficient, and compliant clinical research on a global scale.

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