AstraZeneca is a global biopharmaceutical leader focused on innovative medicines for serious diseases. With a strong commitment to science and patient care, we foster a collaborative, inclusive workplace that encourages growth and innovation.
📍 Location: Mumbai, India
📅 Last Date to Apply: July 30, 2025 (Only 7 hours left!)
🔗 Job ID: R-232458
Detailed Job Description
Key Responsibilities:
✔ Clinical Trial Management: Oversee non-interventional studies (local/global) in collaboration with CROs and investigators.
✔ Regulatory Compliance: Ensure adherence to ICH-GCP, SOPs, and local regulations.
✔ Study Documentation: Assist in designing protocols, CRFs, ICFs, and monitoring plans.
✔ Quality Control: Conduct SDV (Source Data Verification), QC reviews, and ensure data reliability.
✔ Budget & Vendor Management: Negotiate costs, manage CROs, and oversee trial budgets.
✔ Publication Management: Ensure compliance with AstraZeneca’s publication policies.
Desired Skills:
- Strong project management in clinical research
- Experience with CRO collaboration & GCP compliance
- Knowledge of trial protocols, data management, and regulatory requirements
Eligibility Criteria
Essential Qualifications:
- Pharm D or equivalent degree
- Experience in clinical trials, observational studies, and publications
Preferred Qualifications:
- Post-graduate degree in a related field
- Prior experience in pharma/CRO-based clinical research
Why Join AstraZeneca?
✅ Innovative Work Environment: Contribute to cutting-edge clinical research.
✅ Career Growth: Lifelong learning and professional development opportunities.
✅ Inclusive Culture: A diverse and collaborative workplace.
✅ Global Impact: Work on life-changing therapies for patients worldwide.
