PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

AstraZeneca: Pharma Data Analyst & Regulatory Affairs Jobs

Published on

Advertisement

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:

  • Developย analytical programsย to optimizeย pharmaceutical sampling distributionย for AstraZeneca brands.
  • Collaborate withย brand teamsย to implement sampling strategies usingย Python, R, SQL, and Big Data (Hadoop, Spark).
  • Manageย sample allocation prioritiesย across brands and therapeutic areas.
  • Utilizeย Veeva CRM data, IQVIA datasets, and PowerBIย for insights.
  • Lead a team to ensureย timely, accurate deliverables.

Eligibility:

  • Bachelorโ€™s/Masterโ€™sย inย Engineering, Data Science, Statistics, or related fields.
  • 2+ yearsย inย pharma/biotech analyticsย or secondary data analysis.
  • 3+ yearsย inย predictive modeling, optimization, and simulation.
  • Proficiency inย Python, R, SQL, Hadoop, and PowerBI.
  • Experience withย Veeva CRM, IQVIA datasets, and sales analyticsย is a plus.

Benefits:

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

๐Ÿ“… Deadline: July 31, 2025


2. Regulatory Affairs Associate I

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

Job Description:

  • Manageย regulatory submissionsย for global drug approvals.
  • Coordinate withย Health Authorities (FDA, EMA)ย for compliance.
  • Handleย document management (Veeva Vault, eTMF, CTIS).
  • Supportย clinical trial submissions (DSUR, EudraCT).
  • Ensureย regulatory complianceย for AstraZeneca products.

Eligibility:

  • Science/Pharmacy graduate.
  • 3-5 yearsย inย pharma regulatory affairs.
  • Experience withย Veeva Vault, EMA/FDA submissions, and CTIS.
  • Strongย project management & documentation skills.

Benefits:

  • Work withย global regulatory teams.
  • Hybrid work flexibility.
  • Training & certification supportย in regulatory compliance.

๐Ÿ“… Deadline: July 30, 2025


How to Apply?

Application Link For Associate (Data Analytics & Sampling Optimization)

Application Link For Regulatory Affairs Associate I

Advertisement

Share This Job

โœ… Job Details Copied!
Ad Popup