Clinical Research Associate Job Opportunity at AstraZeneca
Seeking an opportunity in Clinical Research jobs? Take your next step as a Clinical Research Associate with AstraZeneca in New Delhi, where scientific excellence meets purpose. This role offers an opportunity to contribute to groundbreaking research in one of the world’s most respected biopharmaceutical organizations. Join an AstraZeneca career that empowers you to advance science, improve patient lives, and shape the future of healthcare.
- Job Position: Clinical Research Associate
- Job ID: R-238617
- Location: New Delhi, National Capital Territory of Delhi, India
About the Company
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company engaged in the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. The organization is more than a pharmaceutical company—it is a place where collaboration, innovation, and patient focus drive meaningful impact, including from every Clinical Research Associate on the team.
Job Overview
The Clinical Research Associate (CRA) at AstraZeneca plays a vital role in managing clinical trial activities at investigator sites, ensuring compliance with all regulatory and ethical standards. Based in New Delhi, this position is responsible for supporting study start-up, site monitoring, and ensuring data integrity throughout the clinical trial process.
Key Responsibilities
- Contribute to the selection of potential investigators and study sites as part of your responsibilities as a Clinical Research Associate.
- Conduct Site Qualification Visits, manage study start-up activities, and ensure regulatory submissions are completed accurately.
- Train and advise investigators and site staff on study-related matters, including Risk-Based Quality Management (RbQM) principles.
- Confirm that all site staff complete necessary training, including ICH-GCP, and maintain inspection readiness.
- Participate in Local Study Team (LST) and National Investigator meetings, which are essential for each Clinical Research Associate.
- Initiate, monitor, and close study sites in compliance with AstraZeneca procedural documents.
- Track patient recruitment and study progress; update systems such as CTMS in accordance with study timelines.
- Perform monitoring visits (onsite and remote), Source Data Review (SDR), Case Report Form (CRF) checks, and Source Data Verification (SDV).
- Ensure accurate and timely reporting of Serious Adverse Events (SAEs) and resolution of data queries because as a Clinical Research Associate, precision is key.
- Maintain inspection-ready Investigator Site Files (ISF) and ensure timely uploads of documents to the eTMF.
- Participate in audits and inspections while upholding AstraZeneca’s Code of Ethics and all local, national, and regional regulations.
- Support quality control checks, archiving of essential documents, and ensure compliance with ICH-GCP and company SOPs.
- Collaborate with Local Study Administrators (LSAD) and Clinical Quality Assurance teams as required to enhance your role as a Clinical Research Associate.
So, What’s Next?
Are you ready to bring new ideas and fresh thinking to AstraZeneca? This is your opportunity to make an impact in clinical research and help redefine the future of medicine in the role of a Clinical Research Associate. We look forward to receiving your application before 14 November 2025 and welcoming you to a team that is passionate about innovation and patient care.
A Clinical Research Associate role at AstraZeneca in Delhi offers more than a job—it’s a chance to be part of a global scientific movement that prioritizes innovation, ethics, and patient well-being. With an inclusive culture and a focus on continuous growth, an AstraZeneca career empowers professionals to advance clinical excellence and contribute to meaningful change in healthcare. Apply now to shape your future with one of the world’s most respected biopharmaceutical companies.
