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Pharmacovigilance Intern

Propharma
0-1 years
INR ₹2.5 – ₹4.0 LPA
Hyderabad
10 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Key Responsibilities

Case Intake & Book-In

  • Manage assigned mailboxes and client communications.

  • Perform inbox triage of adverse event reports.

  • Conduct duplicate searches.

  • Complete initial case book-in activities.

Data Entry & Case Processing

  • Enter safety data into the Argus database.

  • Capture patient information, reporter details, suspect products, and adverse events.

  • Support case processing activities and follow-up management.

Medical Review Support

  • Assist with narrative writing.

  • Perform MedDRA coding.

  • Support quality review activities.

Regulatory Compliance

  • Assist in Individual Case Safety Report (ICSR) management.

  • Ensure compliance with global pharmacovigilance regulations.

  • Maintain accurate documentation and audit readiness.

Cross-Functional Collaboration

  • Coordinate with internal teams for timely case processing.

  • Support regulatory reporting requirements.


Required Skills

Technical Skills

  • Argus Safety Database

  • Adverse Event Processing

  • ICSR Management

  • MedDRA Coding

  • Narrative Writing

  • Pharmacovigilance Fundamentals

Software Skills

  • Microsoft Excel

  • Microsoft Word

  • Microsoft PowerPoint

Soft Skills

  • Attention to Detail

  • Analytical Thinking

  • Communication Skills

  • Time Management

  • Team Collaboration


Preferred Knowledge

  • Pharmacovigilance regulations and guidelines

  • Drug safety reporting requirements

  • Case processing workflows

  • Medical terminology

  • Clinical research basics