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About the role
- Associate Manager overseeing global study delivery for clinical research projects at AstraZeneca, collaborating with internal teams and external providers to ensure efficiency and compliance.
Responsibilities
- In partnership with AZ enablement team, ensures study delivery.
- Leads/contributes to preparation of delegated study documents.
- Maintains internal and external interactions to ensure efficient study delivery.
- Contributes to planning and conduct of internal/external meetings.
- Ensures supply of Investigational product and study materials.
- Contributes to risk and issue identification and development of mitigation plans.
- Ensures study documents in scope are complete and verified for quality.
- Supports Global Study Leader with budget management and invoice reconciliation.
- Adheres to global clinical processes and international guidelines to ensure inspection readiness.
Requirements
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably at least 3 years.
- Knowledge of clinical development / drug development process in various phases of development and therapy areas.
- Excellent knowledge of international guidelines ICH/GCP.
- Good project management skills.
- Demonstrated ability to collaborate as well as work independently.
- Computer proficiency, advanced computer skills in day-to-day tasks.
- Basic knowledge of GXP outside of GCP (i.e GMP/GLP).
Benefits
- AstraZeneca embraces diversity and equality of opportunity.
- We are committed to building an inclusive and diverse team representing all backgrounds.
- We have a promise to you: to help you realise the full breadth of your potential.
- Commitment to lifelong learning, growth and development for all.
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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