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Clinical Supply Manager Job Details | LEO Pharma LEO Pharma uses its own cookies as well as cookies from third parties. Cookies and the related processing of your personal data are used to remember your settings, traffic metrics, to present you with targeted adverts, and to track your use of our website. You may withdraw or change your consent by clicking on the cookie-icon at the bottom left of this website. Your consent covers the use of cookies and the related processing of your personal data. You may read more on our use of cookies here and about our cookie policies here. Your career Clinical Supply Manager Field of work: Clinical Development Posting Date: 17 Jul 2026 Location: Gdansk 80-309, Poland Contract type: Permanent Job ID: 4482 Role Description Do you want to play a critical role in bringing new medicines to patients worldwide? Are you motivated by ownership, complexity, and global collaboration? We are looking for a Clinical Supply Manager to lead end‑to‑end clinical trial supply activities across international clinical studies. You will work closely with cross‑functional teams, external partners, and global stakeholders, taking responsibility for planning, execution, and continuous improvement of clinical supply operations. Join us in creating a future legacy in medical dermatology At LEO Pharma, we are global leaders in medical dermatology. We have 115 years’ experience in bringing innovation to healthcare. And we are eager to do much more. Each year, close to 100 million people have a better day because of our medicines . In Clinical Trial Supply Management, we share a “challenge accepted” mindset and are guided by our winning behaviours of simplification, collaboration, and accountability, to achieve our goals. Your role As a Clinical Supply Manager, you will lead end‑to‑end clinical trial supply activities across global clinical studies. Your key responsibilities include: • Planning, coordinating, and managing clinical trial supply timelines in collaboration with internal teams and external partners • Leading end‑to‑end clinical supply management including IMP, non‑IMP, comparator, and ancillary sourcing, forecasting, waste reduction, handling, and destruction • Managing budgets, forecasts, RFPs, service requests, and approve study‑related invoices • Overseeing labeling, packaging, distribution, import/export, and external packaging facilities in compliance with GMP, GDP, and GCP requirements • Acting as IRT lead, responsible for system setup, execution, reconciliation, and close‑out • Ensuring protocol consistency from a trial supplies perspective • Developing, reviewing, and approving SOPs and trial documentation in line with internal procedures and regulatory requirements • Serving as a subject‑matter expert in biological IMPs and temperature deviation management • Participating in and presenting at global Investigator and Monitor Meetings • Leading optimization and improvement projects to support Global Clinical Operations Your qualifications To succeed in this role, we imagine that you have the following qualifications: • MSc in Pharmacy, or related scientific field • Several years of professional experience within the pharmaceutical industry • Proven experience in IRT system handling having worked with some key vendor systems of today • Forecasting lead experience at driving new projects for supply and demand of IMP globally • Experience in the implementation of new processes/ SOPs • Experience in Quality event management & IMP audit/ inspections • Bulk ordering & depot distribution experience • Experience supporting clinical trials across different geographic markets • Strong knowledge of GMP, GDP, and GCP • Strong analytical, organizational, and problem‑solving skills • Effective communicator with resilience in a fast‑paced environment • Proven ability to build relationships and work across cultures • Fluent in written and spoken English • Strong IT proficiency Contact and Application Your application If this exciting opportunity aligns with your expertise, we’d love to hear from you! You do not need to upload a cover letter, but feel free to include a few sentences in your CV about why this position excites you. Please refrain from adding a photo to your CV. Beyond the skin Join LEO Pharma, a global leader in medical dermatology, as we go beyond the skin to make a lasting impact. Our innovative approach sets us apart. We are dedicated to leaving a legacy that positively impacts patients, colleagues, and our planet. At LEO Pharma, we believe in the power of individuals to drive change. Our flat organizational structure empowers you to make a visible impact and offers versatile roles for professional growth. We value diversity and welcome applications from all qualified candidates, recognizing that our different perspectives, backgrounds, and attitudes enable us to make the best decisions. Join our passionate team at LEO Pharma and be yourself as we work together to make a difference. 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