Clinical Research Associate Job | at AstraZeneca, Apply Now
If you’re looking to accelerate your career in clinical research, this Clinical Research Associate job at AstraZeneca Bengaluru offers the perfect opportunity. As part of a world-renowned biopharmaceutical leader, you’ll play a crucial role in managing and supporting clinical studies that drive the next generation of breakthrough medicines. This position is ideal for life sciences professionals eager to grow in global clinical trial management, regulatory documentation, and patient safety operations — all within a collaborative, innovation-driven environment.
- Job Opening: Clinical Research Associate
- Location: Bengaluru, Karnataka, India
- Job ID: R-236736
About The Company
AstraZeneca is a global, science-led biopharmaceutical company committed to delivering life-changing medicines in areas such as oncology, cardiovascular, renal, metabolic, and respiratory diseases. With operations in over 100 countries, AstraZeneca focuses on translating science into therapeutic breakthroughs that improve patient outcomes worldwide. The Bengaluru site serves as a critical hub for clinical operations and data management, offering opportunities for professionals to work with world-class experts, cutting-edge research systems, and an inclusive culture that values curiosity, teamwork, and excellence.
About the Role
AstraZeneca is hiring for an exciting Clinical Research Associate job based in Bengaluru, Karnataka. This role involves managing critical aspects of global clinical studies—from initiation to reporting—ensuring compliance, accuracy, and operational excellence in line with global standards.
Key Responsibilities
For this Clinical Research Associate Job, you will have to:
- Execute study delivery processes and manage the development of study reports and tools.
- Act as the main liaison for clinical-regulatory documentation and coordinate with the Document Management group until study completion.
- Manage and maintain clinical study documents in the Global Electronic Library according to global document lists.
- Collaborate with Data Management teams to facilitate timely document submissions and study material tracking.
- Monitor administrative tasks, audits, and inspections as per regulatory and company standards.
- Serve as a technical expert in Patient Safety, ensuring compliance and quality throughout the study lifecycle.
- Identify opportunities to enhance clinical study methodologies and implement practical process improvements.
Education and Experience
Essential Qualifications required for a Clinical Research Associate Job:
- Bachelor’s degree in a relevant discipline (Life Sciences, Pharmacy, or related field).
- Prior experience in study management or clinical operations.
- Sound understanding of clinical regulations and reporting standards.
Desirable Qualifications required for a Clinical Research Associate:
- Advanced degree or professional certification in clinical research.
- Comprehensive understanding of study management processes.
Why Join AstraZeneca?
AstraZeneca offers more than just a Clinical Research Associate job — it’s an opportunity to contribute to groundbreaking clinical trials and advance global healthcare. As part of a world-renowned team in the clinical research industry, you’ll gain exposure to innovative study management tools, diverse global collaborations, and a workplace that celebrates diversity and inclusion.
