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AstraZeneca: Pharma Data Analyst & Regulatory Affairs Jobs

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AstraZeneca is a global biopharmaceutical leader committed to transforming patient lives through innovative medicines. With a strong presence in Bangalore, India, the company focuses on drug development, data analytics, and regulatory compliance. AstraZeneca fosters a collaborative, inclusive work culture with opportunities for professional growth, cutting-edge research, and global impact.


Job Openings in Bangalore

1. Associate (Data Analytics & Sampling Optimization)

Job ID: R-232237 | Location: Bangalore | Career Level: C2

Job Description:

  • Develop analytical programs to optimize pharmaceutical sampling distribution for AstraZeneca brands.
  • Collaborate with brand teams to implement sampling strategies using Python, R, SQL, and Big Data (Hadoop, Spark).
  • Manage sample allocation priorities across brands and therapeutic areas.
  • Utilize Veeva CRM data, IQVIA datasets, and PowerBI for insights.
  • Lead a team to ensure timely, accurate deliverables.

Eligibility:

  • Bachelor’s/Master’s in Engineering, Data Science, Statistics, or related fields.
  • 2+ years in pharma/biotech analytics or secondary data analysis.
  • 3+ years in predictive modeling, optimization, and simulation.
  • Proficiency in Python, R, SQL, Hadoop, and PowerBI.
  • Experience with Veeva CRM, IQVIA datasets, and sales analytics is a plus.

Benefits:

  • Competitive salary & performance bonuses.
  • Hybrid work model (3 days in-office).
  • Career growth in global pharma analytics.
  • Access to cutting-edge AI/ML tools.

📅 Deadline: July 31, 2025


2. Regulatory Affairs Associate I

Job ID: R-232198 | Location: Bangalore | Career Level: C1

Job Description:

  • Manage regulatory submissions for global drug approvals.
  • Coordinate with Health Authorities (FDA, EMA) for compliance.
  • Handle document management (Veeva Vault, eTMF, CTIS).
  • Support clinical trial submissions (DSUR, EudraCT).
  • Ensure regulatory compliance for AstraZeneca products.

Eligibility:

  • Science/Pharmacy graduate.
  • 3-5 years in pharma regulatory affairs.
  • Experience with Veeva Vault, EMA/FDA submissions, and CTIS.
  • Strong project management & documentation skills.

Benefits:

  • Work with global regulatory teams.
  • Hybrid work flexibility.
  • Training & certification support in regulatory compliance.

📅 Deadline: July 30, 2025

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How to Apply?

Application Link For Associate (Data Analytics & Sampling Optimization)

Application Link For Regulatory Affairs Associate I

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