Associate Director, Cell Therapy Learning Lead

aerzteforum.info

Not specified (potentially hybrid based on industry standards).
7 years operational experience in drug development
Strong knowledge of ich gcp fda ema regulations
Experience working with internal and external partners
The Associate Director, Cell Therapy Learning Lead at AstraZeneca will oversee the development of learning materials for Cell Therapy procedures, ensuring compliance and quality in clinical trials. The role demands extensive experience in drug development and strong collaborative skills to support various teams in maintaining high operational standards

Job Summary

  • The role is responsible for overseeing and leading the development of learning materials specifically for Cell Therapy procedures.
  • This position serves as the first line of quality support to ensure all trials are prepared for internal and external audits.
  • The incumbent must collaborate closely with Process Owners to ensure established processes adhere to AstraZeneca global quality standards.

Matching Summary

Match Score: 85

The Associate Director, Cell Therapy Learning Lead at AstraZeneca will oversee the development of learning materials for Cell Therapy procedures, ensuring compliance and quality in clinical trials. The role demands extensive experience in drug development and strong collaborative skills to support various teams in maintaining high operational standards.

Skills & Requirements

Must-have

  • 7 years operational experience in drug development
  • Strong knowledge of ICH GCP FDA EMA regulations
  • Experience working with internal and external partners
  • Proven skills in time management and delivery
  • Demonstrated written and verbal communication skills

Nice-to-have

  • Lean Six Sigma process improvement methodology
  • Strong reputation within the business and industry
  • Growth mindset and innovation focus
  • Experience mentoring and knowledge transfer
  • Conflict management and negotiation skills

Key Requirements

  • Bachelor of Science degree or equivalent experience
  • At least 7 years relevant operational or quality experience
  • Strong knowledge of Clinical Study information systems

Work Rights

Not specified

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