Instagram
youtube
Facebook

Pharmacovigilance Intern

0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Pharmacovigilance Intern

Location: Hyderabad, India (Work from Office)
Department: Pharmacovigilance
Employment Type: Full-Time Internship
Duration: 12 Months
Job Requisition ID: JR 7887
Posted On: Yesterday


About ProPharma

For over 20 years, ProPharma has been dedicated to improving patient health and wellness. We provide expert consulting solutions that empower biotech, medical device, and pharmaceutical organizations to confidently advance scientific breakthroughs and bring new therapies to market.

Our advise-build-operate model supports the entire product lifecycle with services in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


About the Role

We are offering an exciting internship opportunity in the Pharmacovigilance Department for individuals with prior experience in the Argus Safety Database. This role will provide hands-on experience in drug safety processes, case management, and regulatory reporting, laying the foundation for a strong career in pharmacovigilance.


Key Responsibilities

  • Manage assigned mailboxes (inbox triage for client communication, inbound reports, internal case communications).

  • Perform duplicate searches and complete initial book-in as required.

  • Enter key data into the Argus safety database (patient details, report, suspect drug, adverse event).

  • Assist in case processing and follow-ups within the Argus database.

  • Support narrative writing and MedDRA coding.

  • Contribute to Individual Case Safety Report (ICSR) management ensuring regulatory compliance.

  • Collaborate with cross-functional teams for timely adverse event reporting.

  • Maintain accurate documentation while adhering to pharmacovigilance compliance standards.


Requirements

  • Degree in Pharmacy, Life Sciences, Medicine, or related field.

  • Basic knowledge and prior training/experience in Argus Safety Database (mandatory).

  • Understanding of pharmacovigilance principles and drug safety regulations.

  • Strong attention to detail and analytical skills.

  • Ability to work effectively in a fast-paced environment.

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

  • Excellent verbal, written, and interpersonal communication skills.


What We Offer

  • Hands-on experience in a global pharmacovigilance setting.

  • Exposure to real-world case processing and regulatory requirements.

  • Mentorship and training from industry experts.

  • Enhanced career prospects in drug safety and regulatory affairs.

  • An inclusive, diverse, and collaborative workplace where innovation and authenticity are celebrated.