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Drug Safety Associate Jobs in Hyderabad

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If you are looking to advance your career in pharmacovigilance (PV), this is a strong opportunity for professionals with 2–4 years of experience in drug safety and case processing. A growing clinical services organization based in Jubilee Hills, Hyderabad is actively hiring Drug Safety Associates for immediate joining.

This role is ideal for candidates with hands-on experience in post-marketing surveillance, ICSR processing, and safety databases like ArisG, along with exposure to global regulatory systems like EudraVigilance.


Key Responsibilities – Drug Safety Associate (PV)

  • Perform end-to-end case processing (ICSR) in compliance with global regulatory requirements
  • Conduct post-marketing surveillance (PMS) activities
  • Work on ArisG safety database for case entry, review, and workflow management
  • Handle EudraVigilance submissions and reporting requirements
  • Manage XML file generation and validation (E2B R2/R3 formats)
  • Ensure data quality, consistency, and regulatory compliance
  • Collaborate with cross-functional teams in clinical safety operations

Eligibility Criteria & Qualifications

  • Education: B.Pharm / M.Pharm / Life Sciences
  • Experience: 2–4 years in Pharmacovigilance
  • Strong understanding of:
    • Case processing & narrative writing
    • GVP guidelines
    • Safety databases (ArisG preferred)
    • EudraVigilance & XML handling
  • Good communication and analytical skills

Required Skills

  • Drug Safety Associate jobs in Hyderabad
  • Pharmacovigilance jobs for 2–4 years experience
  • PV case processing jobs India
  • ArisG safety database experience
  • EudraVigilance XML handling jobs
  • Clinical trial safety operations careers

Work Details

  • Location: Hyderabad (Jubilee Hills)
  • Interview Mode: Face-to-Face only (No virtual interviews)
  • Joining: Immediate joiners preferred

Salary & Benefits (Estimated)

  • 💰 Salary Range: ₹4.5 LPA – ₹7.5 LPA (based on experience & skillset)
  • Opportunity to work with a new-age clinical services organization
  • Exposure to:
    • Clinical Trial Safety Operations
    • Regulatory Affairs
    • Biostatistics & Clinical SAS Programming
  • Career growth in global pharmacovigilance projects

How to Apply

Interested candidates can apply by sending their updated CV to:

📩 Careers@thereqrootr.com
📌 Subject Line: Application for Drug Safety Associate – Pharmabharat

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