Clinical Study Administrator

Typical Accountabilities:

• Provides technical expertise to clinical trials staff within AstraZeneca within the area of study management

• Supports with the administrative aspects of the study process

• Works within establish frameworks to deliver a variety of tasks that support projects in meeting their objectives

• Conducts a wide range of often complex study management enablement processes on an individual basis

• Reviews the development and validation of methods for study management enablement protocols and ensures they are adequate and compliant with clinical trials and AstraZenca standards

• Maintains the documentation of findings and outcomes to meet internal and external requirements

• Keeps own knowledge of best practices and new relevant developments by learning from senior management

• Analyses information to determine project requirements and resolves queries project teams have

• Reviews working practices and ensures non-compliant processes are escalated

• Ensures own work is compliant within Clinical Development

Typical People Management Responsibility (direct / indirect reports):

• Approximate number of people managed in total (all levels) - 0

What is the global remit? (how many countries will the role operate in?):

• Own country

Education, Qualifications, Skills and Experience:

• Essential: Bacherlor’s Degree; Knowledge of any relevant legislation and new developments in the area of clinical development
• Desirable: Working towards a professional qualification; Experience within the pharmaceutical industry; Experience in supporting clinical trials and study development

Key Relationship to reach solutions:

• Internal (to AZ or team): Study management function; Other AstraZeneca employees
• External (to AZ): External service providers and regulatory bodies