Clinical Research Associate

Location: Bengaluru, Karnataka, India
Job ID: R-234758
Closing Date: 29-Sept-2025

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company driven by innovation in the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. More than a leading pharmaceutical company, AstraZeneca is committed to transforming healthcare and improving patient outcomes worldwide.

Role Overview

As a Clinical Research Associate (CRA) at AstraZeneca, you will play a vital role in ensuring the delivery and compliance of clinical studies. You will manage study documents, liaise with internal and external stakeholders, and support clinical research processes from start-up through to reporting.

This is an excellent opportunity for professionals with a clinical research background who want to be part of a collaborative, diverse, and innovative environment.

Key Responsibilities

• Execute study delivery processes through study reports, tools, and systems.
• Provide expert support for centrally managed study services across clinical studies.
• Serve as the main contact for document management until finalization of the Clinical Study Report.
• Maintain production of study documents, ensuring compliance with templates and versions.
• Import and manage clinical-regulatory documents in the Global Electronic Library.
• Collaborate with Data Management teams to facilitate study-related documents.
• Track study materials and equipment across different stages.
• Support audits, inspections, and regulatory processes.
• Act as a technical owner in Patient Safety, ensuring adherence to processes and internal regulations.
• Continuously update knowledge on best practices and regulatory developments.
• Partner with compliance teams to enhance regulatory processes.
• Identify and implement improvements in study methodology.

Qualifications & Experience

Essential:

• Bachelor’s degree in a relevant discipline.
• Experience in study management within a pharmaceutical or clinical background.
• Knowledge of clinical development regulations and industry practices.

Desirable:

• Advanced degree in life sciences or a related field.
• Professional certification in clinical research or study management.
• Broad understanding of multiple aspects of study management.

Key Relationships

• Internal: Study management function, AstraZeneca colleagues.
• External: Regulatory authorities, service providers.

Why Join AstraZeneca?

At AstraZeneca, we are committed to being a Great Place to Work. You’ll be empowered to innovate, push scientific boundaries, and shape the future of healthcare. We foster an inclusive culture that champions diversity, collaboration, learning, and growth. Here, your work truly makes a difference to patients, medicine, and society.

🔗 Apply Now to be part of AstraZeneca’s exciting journey and contribute to pioneering the future of healthcare.