job title: Pharmacovigilance intern (propharma)

Roles and Responsibilities

Key Responsibilities:

• Manage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications.

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

• Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event.

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

• Assist in Narrative Writing, MedDRA Coding.

• Support in Individual Case Safety Report (ICSR) management, ensuring compliance with regulatory requirements.

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

• Maintain accurate documentation and adhere to pharmacovigilance compliance standards.

Requirements:

• Completed a degree in Pharmacy, Life Sciences, Medicine, or a related field.

• Basic knowledge and prior training/experience with Argus safety database is required.

• Understanding of pharmacovigilance principles and drug safety regulations.

• Strong attention to detail, analytical skills, and ability to work in a fast-paced environment.

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

• Strong 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.

• Opportunity to enhance career prospects in drug safety and regulatory affairs.