AstraZeneca
Published on: 28th June 2025
Position/Role: Clinical Research Associate (CRA)
Eligibility: Freshers and Experienced (0–3 years)
Qualification: B.Pharm / M.Pharm / Pharm.D
Location: Karnataka, India
🌐 Application Mode: Online Application via Official Website
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🏢 About AstraZeneca
AstraZeneca is a globally renowned, science-driven biopharmaceutical company with operations in over 100 countries. The company is at the forefront of innovation in oncology, cardiovascular, renal, metabolism, and respiratory diseases. AstraZeneca is committed not just to delivering life-changing medicines but also to creating lasting impact in global healthcare through its investments in research, talent development, and clinical advancement.
📌 Position Overview: Clinical Research Associate (CRA)
Key Responsibilities:
Participate in investigator site selection and feasibility assessments
Conduct Site Qualification, Initiation, Monitoring, and Close-Out Visits (on-site and remote)
Support regulatory documentation, EC/IRB submissions, and site compliance
Train site staff in ICH-GCP, RbQM, and protocol adherence
Monitor patient recruitment, ensure timely SAE reporting, and resolve queries
Maintain Inspection-Ready Site Files (ISF) and ensure eTMF compliance
Collaborate with Local Study Teams (LST) for efficient trial execution
Assist in audit preparation and innovation in trial processes
📋 Hiring Process:
📝 Online Application Only
🔗 Apply via the AstraZeneca Careers Portal (link above)
✅ Eligibility & Experience Criteria:
Educational Qualification: B.Pharm, M.Pharm, or Pharm.D
Experience: 0 to 3 years (Freshers encouraged to apply; prior CRA experience preferred)
Skills:
Strong understanding of ICH-GCP and clinical trial operations
Excellent communication, problem-solving, and coordination skills
Willingness to travel to study sites as required
📎 How to Apply:
Interested candidates should apply through the official AstraZeneca careers page linked above. Ensure the following before submission:
Updated Resume
Educational Certificates
Professional Experience Documents (if applicable)
Valid ID Proof