Clinical Drug Supply Manager (Pharmaceuticals, Hybrid)

Job summary

This role involves managing the execution of clinical drug supply strategies within a dynamic environment, ensuring timely delivery of clinical trial supplies to support innovative cancer treatments and serious diseases.

Qualifications

• Bachelor’s degree or equivalent in a relevant field.
• Experience in the pharmaceutical or biotechnology industry.
• Minimum of 3 years in clinical trial management or clinical drug supply activities is preferred.
• Knowledge of GCP, GMP, and GDP regulations.

Responsibilities

• Oversee end-to-end clinical trial execution from start to finish.
• Maintain up-to-date project and trial information to support drug supply strategies.
• Ensure timely planning and delivery of clinical trial supplies aligned with study milestones.
• Manage trial-level inventory to prevent stock shortages.
• Participate in Clinical Trial Team activities to ensure aligned planning and execution.
• Identify risks related to drug supply and develop mitigation plans.
• Manage project documentation and ensure compliance with regulatory guidelines.
• Support audit preparations and participate in internal improvement projects.

Skills

• Strong communication skills in English, both written and verbal.
• Ability to work effectively under tight deadlines in a fast-paced environment.
• Proactive and goal-oriented with strong prioritization skills.
• Collaborative team player with experience in stakeholder management.

Education

• Bachelor’s degree or equivalent in a relevant discipline.

Tools

• Familiarity with IRT systems and budgeting processes.