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Pharmacovigilance Intern

Propharma
Propharma
0-1 years
Not Disclosed
Hyderabad, India
10 March 10, 2026
Job Description
Job Type: Full Time 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

Job Title: Pharmacovigilance Intern
Company: ProPharma
Location: Hyderabad, India (Work from Office)
Job Type: Full-Time Internship
Duration: 12 Months
Department: Pharmacovigilance / Drug Safety
Job ID: JR 7887
Experience Required: Fresh Graduates or Candidates with Basic Argus Safety Database Training

About ProPharma
ProPharma is a global consulting organization supporting pharmaceutical, biotechnology, and medical device companies throughout the product lifecycle. For over 20 years, ProPharma has helped organizations advance scientific innovation by providing expert solutions across regulatory sciences, clinical research, pharmacovigilance, medical information, quality and compliance, and research and development technology. Through its advise-build-operate model, ProPharma partners with clients to accelerate drug development programs while ensuring regulatory compliance and patient safety.

Role Overview
ProPharma is offering a Pharmacovigilance Internship for graduates interested in developing a career in drug safety and regulatory compliance. This 12-month internship provides hands-on experience in pharmacovigilance operations, including safety case management, adverse event reporting, and regulatory documentation. Interns will gain practical exposure to global safety processes while working with experienced pharmacovigilance professionals and industry-standard safety databases such as Oracle Argus.

Key Responsibilities

Safety Case Intake and Data Management

  • Manage assigned safety mailboxes and perform initial triage of client communications and incoming safety reports.

  • Conduct duplicate case searches and perform initial case book-in activities.

  • Enter essential safety information into the safety database, including patient details, reporter information, suspect drug data, and adverse event details.

Case Processing Support

  • Assist in pharmacovigilance case processing activities within the Argus Safety Database.

  • Support follow-up activities for incomplete or additional safety information related to adverse event reports.

  • Contribute to maintaining accurate and complete case records within safety systems.

Narrative Writing and Medical Coding

  • Assist with narrative writing for Individual Case Safety Reports (ICSRs).

  • Support MedDRA coding of adverse events and medical terms under supervision of pharmacovigilance professionals.

Regulatory Safety Reporting

  • Support ICSR management processes to ensure compliance with global pharmacovigilance regulations.

  • Collaborate with safety and regulatory teams to facilitate timely adverse event reporting.

Documentation and Compliance

  • Maintain accurate documentation of pharmacovigilance activities according to company procedures and regulatory requirements.

  • Ensure adherence to Good Pharmacovigilance Practices (GVP) and internal quality standards.

Educational Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, Medicine, or a related scientific discipline.

Experience Requirements

  • Fresh graduates or candidates with basic training or internship experience in pharmacovigilance.

  • Basic knowledge or training in the Oracle Argus Safety Database is required.

Required Skills and Competencies

  • Understanding of pharmacovigilance principles and drug safety reporting processes.

  • Basic knowledge of adverse event reporting and regulatory compliance requirements.

  • Strong analytical thinking and attention to detail.

  • Ability to work efficiently in a fast-paced and collaborative environment.

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

  • Strong written, verbal, and interpersonal communication skills.

Learning Opportunities

  • Practical exposure to real-world pharmacovigilance case processing and safety reporting.

  • Hands-on experience with industry-standard pharmacovigilance databases and regulatory workflows.

  • Mentorship and guidance from experienced pharmacovigilance professionals.

  • Opportunity to develop skills relevant to careers in drug safety, regulatory affairs, and clinical research.

Work Location
Hyderabad, India (Work from Office).