Not specified (assumed hybrid based on industry norms).
Etmf setup and maintenance
Ich/gcp compliance
Regulatory document collection
AstraZeneca is seeking a Global Study Associate to support Global Study Leaders and manage administrative tasks related to clinical trials. The ideal candidate will possess strong organizational and analytical skills, relevant educational background, and the ability to work both independently and collaboratively
Job Summary
Support Global Study Leaders and Managers by completing delegated study work and leading the set-up, maintenance, and closure of the electronic Trial Master File (eTMF) to ensure compliance.
Collaborate with internal staff and external vendors to collect essential documents, contribute to electronic submissions, and manage clinical-regulatory documents according to technical standards.
Coordinate administrative tasks, logistic support, and practical arrangements for meetings and inspections, while also contributing to process improvements and leading improvement projects.
Matching Summary
Match Score: 85
AstraZeneca is seeking a Global Study Associate to support Global Study Leaders and manage administrative tasks related to clinical trials. The ideal candidate will possess strong organizational and analytical skills, relevant educational background, and the ability to work both independently and collaboratively.
Skills & Requirements
Must-have
eTMF setup and maintenance
ICH/GCP compliance
Regulatory document collection
Clinical study document production
AstraZeneca tracking tools
Clinical Trial Transparency support
Nice-to-have
Process improvement leadership
Training others on procedures
Professionalism and mutual respect
Diverse and inclusive team environment
Key Requirements
Education in medical or biological sciences
Proven organizational and analytical skills
Previous administrative training/experience
Computer proficiency
Working knowledge of Clinical Study Process
Excellent verbal and written English communication