AstraZeneca Hiring Freshers & Experienced in Pre - Clinical Data Management Role

 


🚨 AstraZeneca Hiring Freshers & Experienced in Pre-Clinical Data Management

📅 Published on: June 12, 2025
🏢 Company: AstraZeneca
📍 Location: Bangalore
🎓 Qualifications: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
💼 Experience: 0 - 3 Years
💰 Salary Range: ₹4 - ₹7 LPA
Verified Job | Online Application


🌟 About AstraZeneca

AstraZeneca is a global biopharmaceutical leader pushing the boundaries of science to deliver life-changing medicines. Focused on innovation in oncology, cardiovascular, renal & metabolic diseases, and respiratory & immunology, AstraZeneca fosters a culture of curiosity, inclusion, and lifelong learning.


🧬 Job Role: Nonclinical SEND Data Associate

As a Nonclinical SEND Data Associate, you'll play a pivotal role in standardizing and managing nonclinical study data in alignment with CDISC SEND standards. This position is essential for ensuring regulatory submissions meet global compliance standards such as FDA, ICH, and GLP.


🔍 Key Responsibilities

  • Ensure SEND-compliant datasets for nonclinical studies.
  • Maintain metadata libraries and enforce data standards.
  • Implement updates to CDISC SEND standards.
  • Collaborate with external vendors on data compliance.
  • Perform quality validation of datasets.
  • Support data warehousing, visualization, and submission readiness.
  • Train internal teams on SEND guidelines and tools.
  • Work with LIMS and SEND software solutions.

🎓 Required Qualifications & Experience

Essential Skills:

  • Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
  • 0–3 years of experience in a scientific or regulatory data environment.
  • Understanding of CDISC SEND, FDA, ICH, GLP, and PhUSE guidelines.
  • Proficiency with LIMS and SEND tools.
  • Excellent communication in English (written and verbal).

Desirable:

  • Experience in regulatory submissions within pharma/biotech.


💼 Why Join AstraZeneca?

  • 🌐 Global Impact: Contribute to treatments that improve millions of lives.
  • 💡 Innovative Culture: Work with pioneers in regulatory and drug development.
  • 🏡 Hybrid Model: Minimum 3 days/week in office with flexible work options.
  • 📈 Career Growth: Ongoing training and career development programs.


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