Pharmacovigilance Intern

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Job Title: Pharmacovigilance Intern

Location: Hyderabad (Work from Office)
Duration: 12 Months
Department: Pharmacovigilance

About the Role:

We are offering an exciting internship opportunity in the Pharmacovigilance department for individuals with experience in the Argus safety database. This role will provide hands-on experience in drug safety processes, case management, and regulatory reporting, helping interns build a strong foundation in pharmacovigilance.

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.