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Pharmacovigilance Intern – Drug Safety Internship Opportunity In Hyderabad

Propharma
Propharma
0 years
Not Disclosed
Hyderabad
2 May 7, 2026
Job Description
Job Type: Internship Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Pharmacovigilance Intern – Drug Safety Internship Opportunity in Hyderabad

Company: ProPharma
Job Title: Pharmacovigilance Intern
Location: Hyderabad, India
Work Mode: Work From Office
Job Type: Full-Time Internship
Internship Duration: 12 Months
Department: Pharmacovigilance
Job ID: JR 7887


About ProPharma

ProPharma is a globally recognized life sciences consulting organization specializing in regulatory sciences, pharmacovigilance, clinical research, quality compliance, medical information, and R&D technology solutions. For over 20 years, ProPharma has supported pharmaceutical, biotechnology, and medical device companies in accelerating product development and improving patient safety worldwide.


Job Overview

ProPharma is hiring a Pharmacovigilance Intern for its Hyderabad office. This internship offers hands-on exposure to global drug safety operations, adverse event reporting, case processing, and pharmacovigilance compliance activities.

The internship is designed for candidates interested in building a long-term career in:

  • Pharmacovigilance
  • Drug Safety
  • Clinical Research
  • Regulatory Affairs
  • ICSR Processing
  • Safety Database Management

Candidates with prior knowledge or training in the Argus Safety Database will have an advantage.


Experience Required

Eligibility

  • Freshers can apply
  • Candidates with internship training or academic exposure to pharmacovigilance are preferred

Preferred Experience

  • Basic knowledge or training in:
    • Argus Safety Database
    • ICSR Processing
    • MedDRA Coding
    • Pharmacovigilance workflows

This opportunity is ideal for:

  • B.Pharm graduates
  • M.Pharm graduates
  • PharmD graduates
  • Life Sciences graduates
  • Candidates starting careers in Drug Safety

Educational Qualification

Candidates must have completed a degree in:

  • Pharmacy
  • Life Sciences
  • Medicine
  • Healthcare or related scientific disciplines

Key Responsibilities

Drug Safety Operations

  • Manage pharmacovigilance mailboxes and client communications
  • Perform inbox triage and adverse event intake activities
  • Conduct duplicate checks for safety cases
  • Support initial case book-in activities

ICSR Processing

  • Enter adverse event data into the Argus Safety Database
  • Assist with:
    • Case processing
    • Follow-ups
    • Safety documentation
    • Narrative writing
    • MedDRA coding

Regulatory Compliance

  • Support Individual Case Safety Report (ICSR) management
  • Ensure compliance with global pharmacovigilance regulations
  • Maintain accurate safety documentation and reporting standards

Cross-Functional Collaboration

  • Work with internal safety teams and stakeholders
  • Support timely adverse event reporting activities
  • Assist in maintaining quality and compliance standards