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    Pharmacovigilance Intern Opportunity – at ProPharma, Apply Now!

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    Pharmacovigilance Intern Opportunity – at ProPharma, Apply Now!

    Looking for a rewarding start in drug safety? Explore this Pharmacovigilance Intern Opportunity at ProPharma in Hyderabad. This 12-month internship offers hands-on experience with the Argus safety database, case processing, and regulatory reporting in a global pharmacovigilance environment.

    • Designation: Pharmacovigilance Intern
    • Location: Hyderabad, India (Work from Office)
    • Duration: 12 Months
    • Department: Pharmacovigilance

    About The Company

    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.

    About the Role

    This Pharmacovigilance Intern Opportunity is ideal for candidates with Argus safety database knowledge who want to gain practical exposure in drug safety. Interns will contribute to case processing, narrative writing, MedDRA coding, and regulatory reporting while building a strong foundation in pharmacovigilance.

    Key Responsibilities

    • Manage assigned mailboxes, including triaging client communication and inbound reports.
    • Perform duplicate searches and initial book-in activities.
    • Enter essential data (patient details, suspect drug, adverse events) into the safety database.
    • Assist in Argus case processing, follow-ups, and narrative writing.
    • Support MedDRA coding and ICSR (Individual Case Safety Report) management.
    • Collaborate with cross-functional teams to ensure timely adverse event reporting.
    • Maintain documentation and ensure compliance with pharmacovigilance standards.

    Requirements

    • Degree in Pharmacy, Life Sciences, Medicine, or related field.
    • Prior training/experience with Argus safety database.
    • Understanding of pharmacovigilance principles and drug safety regulations.
    • Strong analytical skills and attention to detail.
    • Proficiency in Microsoft Office tools.
    • Good verbal, written, and interpersonal communication skills.

    Benefits

    This Pharmacovigilance Intern Opportunity at ProPharma provides:

    • Practical exposure to global pharmacovigilance processes.
    • Training in case management, regulatory requirements, and Argus database use.
    • Mentorship from industry experts.
    • A strong foundation to pursue careers in drug safety and regulatory affairs.

    APPLY ONLINE HERE

    Apply now

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