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GSK Technical Associate Intern 2025 – Pharmacovigilance (Freshers)

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GSK

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Health Sciences

₹25,000 – ₹35,000 per month

Bangalore

Freshers

Verified Job

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Global biopharma leader GSK invites applications for the position of Technical Associate Intern in its Pharmacovigilance Excellence (PVE) team at Bengaluru.
This full-time internship offers hands-on experience in drug safety processes, Veeva Vault management, eTMF support, and global PV operations, making it an ideal opportunity for Life Science and Pharmacy graduates aspiring to build a career in pharmacovigilance and clinical research.


💼 Key Responsibilities

  • Provide cross-functional technical support within the Pharmacovigilance Excellence (PVE) team.
  • Assist Global Process Owners (GPOs) and Safety Process Leads (SPLs) with operational and documentation tasks.
  • Undertake Template Manager role for PV documents in Veeva Vault (Regulatory & Clinical).
  • Support metric collection, management monitoring, and PV communications.
  • Manage group mailboxes and ensure timely triage of technical queries.
  • Review and update PVE web content and documentation repositories.
  • Support Development Core Safety Information (DCSI) management and Case Awareness tools.
  • Provide assistance for eTMF, Medical Devices safety, and MedDRA/TFQ operations.

🎓 Qualifications and Eligibility

  • Bachelor’s degree in Health Sciences, Pharmacy, or Life Sciences (e.g., B.Pharm, M.Pharm, B.Sc, M.Sc in Biotechnology, Biochemistry, Microbiology, etc.)
  • Strong computer proficiency (MS Word, Excel, and document management systems).
  • Familiarity with medical/scientific terminology and PV/clinical processes is desirable.
  • Excellent written and verbal communication skills.
  • High attention to detail, ability to work under tight deadlines, and collaborative mindset.

💰 Salary Range

  • Estimated stipend/salary: ₹25,000 – ₹35,000 per month (based on similar GSK internship programs in India).

🌈 Why Join GSK?

  • Gain exposure to global pharmacovigilance systems and data integrity processes.
  • Work on real-world safety data, contributing to the mission of “getting ahead of disease together.”
  • Inclusive and supportive workplace encouraging professional growth.
  • Opportunity to transition into full-time roles upon performance and business needs.

📝 How to Apply

Application Link

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