Pharmacovigilance Intern
Job ID: JR 8692
Location: India
Employment Type: Full-time
Industry: Pharmacovigilance | Drug Safety | Clinical Safety
About ProPharma
ProPharma is a globally recognized provider of regulatory sciences, pharmacovigilance, clinical research, quality & compliance, medical information, and R&D technology solutions. For over 20 years, ProPharma has partnered with biotech, pharmaceutical, and medical device companies worldwide through its advise–build–operate model, enabling the successful development and safe commercialization of innovative therapies across the complete product lifecycle.
Job Overview
ProPharma is seeking a Pharmacovigilance Intern to support day-to-day drug safety operations and case processing activities. This role is ideal for life sciences graduates or early-career professionals looking to build foundational experience in global pharmacovigilance, adverse event processing, and regulatory safety workflows within a structured, compliance-driven environment.
Key Responsibilities
Manage assigned pharmacovigilance mailboxes, including triage of client communications, inbound adverse event reports, and internal case-processing correspondence.
Perform duplicate searches and complete initial case book-in activities as per established procedures.
Screen and redact source documents to remove protected health information (PHI) in compliance with company and regulatory guidelines.
Support literature surveillance and literature-related pharmacovigilance activities as required.
Conduct initial triage of regulatory authority database searches.
Prepare and share draft adverse event reports with clients for review, as applicable.
Enter basic case information into the safety database, including identifiable patient, reporter, suspect product, and adverse event details.
Perform full case data entry into the safety database following appropriate training and authorization.
Support additional pharmacovigilance operational tasks as assigned.
Required Skills & Competencies
Strong verbal, written, and interpersonal communication skills.
Proficiency in computer applications with good keyboarding skills; familiarity with safety databases is an advantage.
High level of attention to detail with strong organizational and prioritization abilities.
Ability to work independently as well as collaboratively within a team environment.
Willingness to learn and adapt in a regulated, process-driven setting.
Education & Experience Requirements
Education:
Post-secondary education required; degree or ongoing studies in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related discipline preferred.
Experience Required:
0–1 year of experience in pharmacovigilance, clinical research, or pharmaceutical industry operations preferred.
Fresh graduates with relevant academic exposure or internships in drug safety are encouraged to apply.
Diversity & Inclusion
ProPharma is committed to fostering a diverse, equitable, and inclusive workplace where individuals are empowered to contribute authentically. The organization values innovation, collaboration, and professional growth and provides a supportive environment for early-career talent.
Recruitment Process & Notice
All applications to ProPharma are reviewed directly by the recruitment team. The company does not use AI-based screening tools, and all candidates will receive an application outcome. ProPharma Group does not accept unsolicited resumes from recruitment agencies or third parties.
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