Associate Director, Cell Therapy Learning Lead

AstraZeneca

**
7 years operational experience in drug development
Strong knowledge of ich gcp fda ema regulations
Experience working with internal and external partners
** AstraZeneca is seeking an Associate Director, Cell Therapy Learning Lead to oversee the development of learning materials for cell therapy-specific procedures and ensure clinical trial execution excellence. The ideal candidate will have extensive experience in drug development, quality assurance, and strong communication skills to collaborate with both internal and external partners. **

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 adherence to AstraZeneca global quality standards.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director, Cell Therapy Learning Lead to oversee the development of learning materials for cell therapy-specific procedures and ensure clinical trial execution excellence. The ideal candidate will have extensive experience in drug development, quality assurance, and strong communication skills to collaborate with both internal and external partners. **

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
  • Ability to influence across organizational boundaries

Nice-to-have

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

Key Requirements

  • Bachelor of Science degree or equivalent experience
  • At least 7 years relevant operational/quality experience
  • Knowledge of Clinical Study information and technology

Work Rights

Not specified

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