Clinical Project Assistant
SanofiÂ
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Job Description
Location: Hyderabad, India (Work from Office)
Job Requisition ID: JR 7887
Job Type: Full-Time Internship (12 Months)
Department: Pharmacovigilance
About the Role
This internship provides hands-on experience in pharmacovigilance, focusing on drug safety processes, case management, and regulatory reporting. It is designed for individuals with basic knowledge of pharmacovigilance principles and prior exposure to the Argus safety database.
Role & Responsibilities
- Manage pharmacovigilance mailboxes, including triage of client communication, inbound reports, and internal processing.
- Perform duplicate searches and initial book-ins as required.
- Enter key safety data into the Argus database (patient, drug, and adverse event details).
- Support case processing, including follow-ups, narrative writing, and MedDRA coding.
- Assist with Individual Case Safety Report (ICSR) management in compliance with global regulations.
- Collaborate with cross-functional teams to ensure timely adverse event reporting.
- Maintain accurate documentation while adhering to compliance standards.
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Educational Qualification
- Degree in Pharmacy, Life Sciences, Medicine, or a related field (required).
- Basic knowledge and hands-on training with Argus safety database (mandatory).
- Understanding of pharmacovigilance principles and regulatory requirements.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Strong attention to detail, analytical mindset, and ability to work in a fast-paced environment.
- Excellent verbal, written, and interpersonal communication skills.
Location
Hyderabad, India (Work from Office)
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