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Pharmacovigilance Intern

Propharma
Propharma
Freshers years
Not Disclosed
Hyderabad
10 May 6, 2026
Job Description
Job Type: Full Time Internship Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Overview

ProPharma Group has over 20 years of experience improving patient health and wellness by supporting biotech, medical device, and pharmaceutical organizations.

Through its advise–build–operate model, ProPharma delivers end-to-end solutions across the product lifecycle, with expertise in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


Job Title

Pharmacovigilance Intern


Job Details

  • Location: Hyderabad (Work from Office)

  • Duration: 12 Months

  • Department: Pharmacovigilance


Role Summary

This internship offers hands-on experience in pharmacovigilance, focusing on drug safety processes, case management, and regulatory reporting. It is ideal for candidates with prior exposure to the Argus safety database who want to build a strong foundation in drug safety.


Key Responsibilities

1. Case Intake & Mailbox Management

  • Manage assigned mailboxes

  • Perform inbox triage of:

    • Client communications

    • Inbound safety reports

    • Internal case-related communications


2. Case Processing Support

  • Conduct duplicate searches

  • Perform initial case book-in activities

  • Enter basic safety data into the database, including:

    • Patient information

    • Reporter details

    • Suspect drug

    • Adverse events

  • Assist in:

    • Case processing within Argus

    • Follow-up activities


3. Safety Data Handling

  • Support:

    • Narrative writing

    • MedDRA coding

  • Assist in Individual Case Safety Report (ICSR) management

  • Ensure compliance with regulatory reporting requirements


4. Collaboration & Compliance

  • Work with cross-functional teams to ensure timely reporting

  • Maintain accurate documentation

  • Adhere to pharmacovigilance compliance standards


Eligibility Criteria

Education

  • Completed degree in:

    • Pharmacy

    • Life Sciences

    • Medicine

    • Related field


Technical Knowledge

  • Basic knowledge of pharmacovigilance and drug safety regulations

  • Prior training/experience with Argus safety database (mandatory)


Skills & Competencies

  • Strong attention to detail

  • Analytical thinking

  • Ability to work in a fast-paced environment

  • Proficiency in:

    • MS Word

    • MS Excel

    • MS PowerPoint

  • Strong verbal, written, and interpersonal communication skills


What You Will Gain

  • Hands-on experience in a global pharmacovigilance environment

  • Exposure to:

    • Real-world case processing

    • Regulatory reporting requirements

  • Mentorship and training from industry professionals

  • Opportunity to enhance career prospects in:

    • Drug safety

    • Regulatory affairs


Work Culture & Values

  • Commitment to Diversity, Equity & Inclusion

  • Equal Opportunity Employer

  • Encourages innovation, collaboration, and authenticity

  • Supportive and inclusive workplace environment


Important Notice

  • ProPharma does not accept unsolicited resumes from recruiters or third parties

  • No phone calls or emails regarding this role