Clinical Supply Manager

Job summary

The role involves managing clinical supply activities for global phase I-IV clinical trials, supporting the R&D pipeline of drug candidates. You will coordinate supplies from trial design to completion, collaborating with various stakeholders and external vendors.

Qualifications

• Master's degree in pharmacy, engineering, chemistry, industrial medicine, or a related field.
• 3-7 years of experience in Clinical Supply, Clinical Development, Project Management, or similar roles in the pharmaceutical, biotechnology, or medical device industries.
• Experience in clinical supply forecasting and planning.
• Strong stakeholder management skills, both internally and externally.
• Proven experience working with vendors and CROs/CMOs for clinical supplies.
• Excellent problem-solving abilities and the capacity to manage multiple projects with changing priorities.
• Fluent in English, both written and spoken.

Responsibilities

• Coordinate clinical supplies for multiple clinical trials across phases.
• Define outsourced CMO activities, including packaging, labeling, and distribution.
• Develop blinding strategies and supply forecasting.
• Work independently on key assignments while collaborating with a supportive team.
• Engage in project management tasks and enhance specialized knowledge of clinical development.

Skills

• Strong coordination and analytical skills.
• Ability to inspire and motivate colleagues across cultures and organizations.
• Structured approach to project management and problem-solving.

Education

• Master's degree in a relevant field.

Tools

• Experience with Interactive Response Technology (IRT) is a plus.