Clinical Research Jobs at AstraZeneca
Looking to build a rewarding career in the clinical research domain? This Clinical Research Jobs opportunity at AstraZeneca is your gateway to working with a globally renowned biopharmaceutical company. If you are passionate about clinical trials, patient safety, and scientific innovation, this role as a Clinical Research Associate offers the perfect opportunity for life science graduates to grow, learn, and contribute to cutting-edge healthcare advancements.
About the Company
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company engaged in the discovery, development, and commercialization of prescription medicines for serious diseases. The organization emphasizes innovation, collaboration, and improving patient outcomes worldwide.
Job Details:
- Job Title: Clinical Research Associate (CRA)
- Job ID: R-250944
- Application Deadline: May 8, 2026
- Job Type: Full-Time
- Company: AstraZeneca
Role Overview
The Clinical Research Associate (CRA) is responsible for the delivery and oversight of clinical studies at assigned sites. Acting as the primary point of contact, the CRA ensures that studies are conducted in compliance with procedural documents, international guidelines such as ICH-GCP, and local regulations. The role involves close collaboration with the Local Study Team and supports all phases of study execution, from initiation to closure.
Reporting Structure
- Reports to: Director, Site Management & Monitoring (SMM) / Country Head / Associate Director, SMM
- Works closely with: Local Study Team (LST), Local Study Associate Director (LSAD), and other CRAs
Key Responsibilities
- Conduct site qualification visits and support investigator selection
- Manage study start-up activities and regulatory submissions (where applicable)
- Perform site initiation, monitoring, and close-out visits
- Train and support investigators and site staff on study protocols and Risk-Based Quality Management (RbQM) principles
- Ensure sites are inspection-ready and compliant with study requirements
- Monitor patient recruitment and site performance, ensuring timely issue resolution
- Maintain and update Clinical Trial Management Systems (CTMS)
- Manage study supplies, including Investigator Study Files (ISF) and drug accountability
- Conduct remote and on-site monitoring visits as per study plans
- Perform Site Quality Risk Assessments (SQRA) and adjust monitoring strategies
- Collaborate with data management teams to ensure data quality and query resolution
- Ensure accurate and timely reporting of Serious Adverse Events (SAEs)
- Prepare monitoring reports and follow-up documentation
- Support audits and regulatory inspections
- Maintain and upload documents to the electronic Trial Master File (eTMF)
- Ensure compliance with company policies, ethical standards, and regulatory requirements
Educational Qualification
Bachelor’s degree in a related discipline (preferably Life Sciences) or equivalent qualification
Experience & Knowledge
- Understanding of drug development processes
- Knowledge of ICH-GCP guidelines and local regulatory requirements
- Experience in clinical study management, monitoring, and data handling
Key Skills & Competencies
- Strong communication and interpersonal skills
- Attention to detail and quality focus
- Problem-solving and critical thinking abilities
- Ability to manage multiple priorities and meet timelines
- Team collaboration in both in-person and virtual environments
- Learning agility and adaptability
- Ethical mindset with strong integrity
- Ability to travel nationally/internationally (as required)
Stakeholder Interaction
- Internal: Cross-functional teams across Research & Development
- External: Research organizations, investigators, and regulatory authorities
Work Environment
- Dynamic clinical research setting
- Collaborative, global team environment
- Opportunities for continuous learning and career growth
Why Join?
AstraZeneca offers a culture focused on innovation, inclusion, and professional development. Employees are empowered to contribute to meaningful scientific advancements and improve patient outcomes globally.
