Senior Clinical Trial Supply Manager

Job summary

The role involves managing the supply chain for clinical trials, ensuring timely delivery of supplies for global development programs. The Senior Clinical Trial Supply Manager will lead supply strategy and execution for complex trials, collaborating with various stakeholders.

Qualifications

• Over 5 years of experience in clinical trial supply within the pharmaceutical industry.
• In-depth knowledge of clinical trial operations and regulatory requirements (GMP, GDP, GCP).
• Proven ability to independently manage large and complex trial supply projects.
• Experience in supplier and contract manufacturing organization (CMO) management, including budget oversight.
• Strong communication and collaboration skills.
• Proactive and improvement-oriented mindset.
• MSc in pharmaceutical or relevant natural sciences.

Responsibilities

• Lead clinical trial supply management for complex global clinical programs.
• Plan and execute end-to-end clinical trial supply activities for Phase I–IV trials.
• Represent clinical trial supply in cross-functional teams, ensuring alignment across departments.
• Manage suppliers and CMOs, including selection and performance management.
• Ensure compliance with GxP through effective documentation and risk management.
• Drive continuous improvement initiatives and mentor colleagues.

Skills

• Strong leadership and stakeholder management skills.
• Collaborative mindset with a focus on operational excellence.

Education

• MSc in pharmaceutical or other relevant natural sciences.

Tools

• Familiarity with clinical supply records and systems.