Pharmacovigilance Intern
Location: Hyderabad, India (On-site)
Job Type: Full-Time Internship (12 Months)
Experience Required: 0–1 Year (Candidates with Argus Database Exposure Preferred)
Industry: Pharmacovigilance / Drug Safety / Regulatory Affairs
Job ID: JR 7887
About the Role
We are offering a structured and hands-on Pharmacovigilance Internship for candidates looking to build a career in drug safety and regulatory compliance. This role provides practical exposure to real-world pharmacovigilance operations, including case processing, safety database management, and adverse event reporting. The ideal candidate will have foundational knowledge of pharmacovigilance and prior exposure to the Argus safety database.
Key Responsibilities
Manage and monitor assigned mailboxes, including triaging client communications, inbound safety reports, and internal case-related correspondence. Perform duplicate checks and support initial case book-in activities in line with standard procedures. Enter essential safety data into the database, including patient details, suspect drugs, reporters, and adverse events.
Assist in case processing activities within the Argus safety database, including follow-ups for additional information. Support narrative writing and MedDRA coding to ensure accurate and standardized case documentation. Contribute to the preparation and management of Individual Case Safety Reports (ICSRs) in compliance with global regulatory requirements.
Collaborate with cross-functional teams to ensure timely and accurate adverse event reporting. Maintain high standards of documentation and ensure adherence to pharmacovigilance regulations, SOPs, and data quality requirements.
Required Qualifications
Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, or a related field. Candidates with 0–1 year of experience or prior training/internship in pharmacovigilance are encouraged to apply. Basic knowledge or hands-on exposure to the Argus safety database is required.
Key Skills and Competencies
Strong understanding of pharmacovigilance principles and drug safety processes. High attention to detail with good analytical and problem-solving abilities. Proficiency in Microsoft Office tools such as Word, Excel, and PowerPoint. Effective verbal and written communication skills with the ability to work collaboratively in a team environment. Ability to manage multiple tasks in a fast-paced setting with accuracy and efficiency.
Learning and Career Benefits
This internship provides valuable hands-on experience in a global pharmacovigilance environment, including exposure to case processing workflows, regulatory reporting standards, and safety database systems. Interns will receive mentorship from industry professionals and gain practical skills that enhance career opportunities in pharmacovigilance, drug safety, and regulatory affairs.
About the Organization
The organization is a globally recognized life sciences consulting firm supporting pharmaceutical, biotechnology, and medical device companies across the product lifecycle. With expertise in pharmacovigilance, regulatory sciences, clinical research, and quality compliance, it delivers customized solutions that accelerate innovation and ensure patient safety. The company promotes an inclusive, collaborative, and growth-oriented work environment.
How to Apply
Interested candidates can apply through the official careers portal to begin their career in pharmacovigilance and drug safety.
Uttar Pradesh :
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Siliguri |Illinois :
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Koropi | Athens |Greece :
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Croatia |Zagreb :
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Tallinn |Hà Nội :
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Kyiv |Lima Region :
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