Pharmacovigilance Intern – Drug Safety Operations
Company: ProPharma Group
Location: India
Employment Type: Full-Time
Job Requisition ID: JR 8692
Experience Level: Internship / Entry Level
Experience Required: 0–1 year (Industry experience preferred)
Posted On: 15 days ago
Company Overview
ProPharma Group is a leading global provider of regulatory sciences, clinical research solutions, pharmacovigilance, medical information, quality & compliance, and R&D technology services. With over 20 years of industry expertise, ProPharma partners with biotechnology, medical device, and pharmaceutical organizations worldwide to advance innovation and bring safe, effective therapies to patients through its advise–build–operate model.
Role Overview
ProPharma is seeking a motivated Pharmacovigilance Intern to support drug safety and case processing activities across global client programs. This role offers hands-on exposure to pharmacovigilance operations, safety databases, regulatory processes, and adverse event reporting in a highly regulated healthcare environment. It is an excellent opportunity for graduates or early-career professionals looking to build a career in drug safety and pharmacovigilance.
Key Responsibilities
Manage assigned mailboxes, including triaging client communications, inbound safety reports, and internal case-processing emails.
Perform duplicate case searches and complete initial case intake (book-in) activities as required.
Screen and redact source documents to remove Protected Health Information (PHI) in compliance with company procedures.
Support literature screening and literature-related pharmacovigilance activities as needed.
Conduct initial triage of regulatory authority database searches.
Prepare and send draft safety reports to clients for review, as applicable.
Enter basic safety information into pharmacovigilance databases, including identifiable patient details, reporter information, suspect drug(s), and adverse events.
Perform full case data entry into safety databases following appropriate training and supervision.
Support additional pharmacovigilance and administrative tasks as assigned.
Experience Required
0 to 1 year of experience in pharmacovigilance, drug safety, clinical research, or a related healthcare domain.
Prior internship or industry exposure in pharmacovigilance or safety operations is preferred but not mandatory.
Educational Qualifications
Post-secondary education in Pharmacy, Life Sciences, Clinical Research, Biotechnology, or a related discipline.
Required Skills & Competencies
Strong verbal, written, and interpersonal communication skills.
Good computer proficiency, including keyboarding and use of standard office applications.
High attention to detail with strong organizational and prioritization abilities.
Ability to work independently as well as collaboratively within a team environment.
Willingness to learn pharmacovigilance regulations, safety databases, and SOP-driven workflows.
Diversity, Equity & Inclusion
ProPharma Group is committed to building a diverse, inclusive, and equitable workplace where every employee can thrive. The organization encourages innovation, collaboration, and professional growth while providing a safe and respectful working environment.
Recruitment Process Transparency
All applications are personally reviewed by ProPharma’s recruitment team. The company does not use automated AI screening tools and ensures that every applicant receives a clear outcome of their application.
Important Notice
ProPharma Group does not accept unsolicited resumes from third-party recruiters. Please do not contact company employees directly regarding this vacancy.
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