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Pharmacovigilance Intern

Propharma
Propharma
Fresher years
2-5 LPA
Remote, India, India
50 April 27, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, GCP guidelines, ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, Medical Terminology, Narrative Writing, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Intern – Drug Safety & ICSR Management

Location: Hyderabad, India (Work from Office)
Company: ProPharma Group
Job Type: Full-Time Internship (12 Months)
Job ID: JR 7887
Experience Required: Freshers with prior training/knowledge of Argus Safety Database preferred


About the Company

ProPharma Group is a globally recognized life sciences consulting organization with over two decades of expertise in supporting pharmaceutical, biotechnology, and medical device companies. The organization operates across the complete product lifecycle using an advise-build-operate model, offering specialized solutions in pharmacovigilance, regulatory sciences, clinical research, and quality compliance.

With a strong global presence and domain-driven expertise, ProPharma enables organizations to accelerate drug development while ensuring regulatory excellence and patient safety.


Role Overview

This Pharmacovigilance Internship offers a structured entry point into the drug safety domain. The role is designed for candidates who want hands-on exposure to real-world pharmacovigilance operations, including ICSR processing, Argus database handling, and regulatory compliance.

Interns will gain practical experience working on safety data, case processing workflows, and cross-functional collaboration within a global pharmacovigilance environment.


Key Responsibilities

  • Manage pharmacovigilance mailboxes including triage of incoming adverse event reports and client communications

  • Perform duplicate checks and initial case book-in activities as per standard workflows

  • Enter and validate critical safety data including patient details, suspect drug, and adverse events in the safety database

  • Assist in case processing activities within Argus Safety Database, including follow-ups and data updates

  • Support narrative writing and MedDRA coding for adverse event cases

  • Contribute to Individual Case Safety Report (ICSR) management in compliance with global regulatory guidelines

  • Collaborate with cross-functional teams to ensure timely and accurate adverse event reporting

  • Maintain documentation in alignment with pharmacovigilance SOPs and compliance standards


Eligibility Criteria

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, or related healthcare field

  • Basic knowledge or prior training in Argus Safety Database is mandatory

  • Understanding of pharmacovigilance concepts, ICSR workflow, and drug safety regulations

  • Strong attention to detail and analytical thinking skills

  • Ability to work in a fast-paced, process-driven environment

  • Proficiency in Microsoft Office tools including Word, Excel, and PowerPoint

  • Good verbal, written, and interpersonal communication skills


What You Will Gain

  • Practical exposure to global pharmacovigilance operations and safety databases

  • Hands-on experience in ICSR processing, narrative writing, and MedDRA coding

  • Understanding of regulatory reporting requirements and compliance frameworks

  • Mentorship from experienced professionals in drug safety and clinical research

  • Strong foundation for career growth in Pharmacovigilance, Drug Safety, and Regulatory Affairs


Diversity and Inclusion Commitment

ProPharma Group fosters a culture of inclusion, innovation, and collaboration. The organization is committed to providing equal opportunities and empowering individuals to thrive in a diverse and supportive work environment.


Application Note

ProPharma Group does not accept unsolicited resumes from third-party recruiters for this role. Direct applications through official channels are encouraged.