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Pharmacovigilance Intern

Propharma
Propharma
0-1 years
Not Disclosed
Hyderabad, India
10 March 2, 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

Pharmacovigilance Intern – Drug Safety Operations

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

About the Organization

ProPharma is a global consulting organization supporting biotechnology, pharmaceutical, and medical device companies across the complete product lifecycle. Through its advise–build–operate model, the organization delivers expertise in regulatory sciences, clinical research, pharmacovigilance, quality and compliance, medical information, and R&D technology. With over two decades of industry experience, ProPharma partners with life sciences companies to accelerate innovation while ensuring regulatory compliance and patient safety.

About the Role

ThePharmaDaily.com invites applications for the position of Pharmacovigilance Intern based in Hyderabad. This 12-month, full-time internship offers hands-on exposure to global drug safety operations, Individual Case Safety Report (ICSR) management, and regulatory reporting processes.

This opportunity is ideal for pharmacy and life sciences graduates who possess foundational knowledge of pharmacovigilance principles and prior exposure to the Argus safety database. Interns will gain real-world experience in adverse event case processing, safety data entry, MedDRA coding, and compliance-driven documentation practices.

Key Responsibilities

  • Manage assigned pharmacovigilance mailboxes, including inbox triage of client communications, inbound safety reports, and internal case-related correspondence

  • Perform duplicate searches and complete initial case book-in procedures

  • Enter essential safety data into the Argus database, including identifiable patient information, reporter details, suspect product, and adverse events

  • Assist in case processing activities within the Argus safety system, including follow-up management

  • Support narrative writing and MedDRA coding activities

  • Contribute to Individual Case Safety Report (ICSR) preparation and tracking in compliance with global regulatory requirements

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

  • Maintain accurate documentation aligned with pharmacovigilance quality and compliance standards

Eligibility & Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, Medicine, or a related discipline (completed)

  • Prior training or basic hands-on experience with the Argus Safety Database (mandatory)

  • Understanding of pharmacovigilance concepts, adverse event reporting, and global drug safety regulations

  • Strong attention to detail and analytical skills

  • Ability to work effectively in a structured, deadline-driven environment

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

  • Strong verbal, written, and interpersonal communication skills

Experience Required

  • 0–1 year of relevant internship, academic project, or entry-level experience in pharmacovigilance or drug safety

  • Candidates with prior exposure to safety databases during coursework or internships will have an advantage

What You Will Gain

  • Practical experience in global pharmacovigilance operations

  • Exposure to real-time case processing and regulatory compliance requirements

  • Mentorship and structured learning from experienced drug safety professionals

  • Career-building opportunity in pharmacovigilance, regulatory affairs, and clinical safety domains

Work Culture & Inclusion

The organization promotes diversity, equity, and inclusion, fostering a workplace environment where professionals are encouraged to contribute innovatively and collaboratively. Employees are empowered to grow in a supportive and compliance-driven global setting.

Application Process

Applications will be screened based on academic qualifications and relevant pharmacovigilance exposure. Shortlisted candidates will be contacted for further evaluation and interview rounds.

This internship is ideal for aspiring pharmacovigilance professionals seeking structured industry exposure in drug safety case processing and regulatory-compliant healthcare operations.