Job Title: Pharmacovigilance Intern
Location: India
Employment Type: Full-Time
Job Requisition ID: JR 8692
For over 20 years, ProPharma has been a trusted global partner in improving patient health and wellness. The company supports biotech, medical device, and pharmaceutical organizations through an advise–build–operate model spanning the entire product lifecycle. With deep expertise in regulatory sciences, clinical research, pharmacovigilance, quality & compliance, medical information, and R&D technology, ProPharma delivers fully customizable, end-to-end solutions that accelerate innovation while minimizing risk for high-impact drug and device programs.
ProPharma is seeking a detail-oriented Pharmacovigilance Intern to support its global Patient Safety and Pharmacovigilance operations. This role offers hands-on exposure to safety case processing, regulatory compliance, and safety database management, making it an excellent opportunity for early-career professionals aiming to build a long-term career in pharmacovigilance and drug safety.
Manage assigned safety mailboxes, including triage of client communications, inbound safety reports, and internal case processing correspondence
Perform duplicate case searches and complete initial case book-in activities
Screen and redact source documents to remove Protected Health Information (PHI) in accordance with company SOPs
Support literature monitoring and literature-related pharmacovigilance activities
Conduct initial triage of regulatory authority database searches
Prepare and send draft safety reports to clients for review, as required
Enter essential safety data into pharmacovigilance databases, including patient, reporter, suspect drug, and adverse event details
Perform full safety case data entry into validated safety databases following appropriate training
Support additional pharmacovigilance and operational tasks as assigned
Strong verbal, written, and interpersonal communication skills
Proficiency in computer applications and accurate keyboarding skills
Excellent organizational and time-management abilities with high attention to detail
Ability to work independently while also collaborating effectively within a team
Strong interest in pharmacovigilance, drug safety, and regulatory compliance
Post-secondary education in Life Sciences, Pharmacy, Medicine, Nursing, or a related discipline
Preferred: Up to 1 year of experience in pharmacovigilance, drug safety, clinical research, or a related pharmaceutical industry role
Fresh graduates with relevant academic exposure or internships in pharmacovigilance are encouraged to apply
ProPharma is committed to fostering a diverse, inclusive, and equitable workplace where every individual can thrive authentically. The organization values innovation, collaboration, and entrepreneurial thinking, providing a supportive environment for professional growth and success.
All applications are personally reviewed by ProPharma’s recruitment team. The company does not use AI-based screening tools and ensures that every applicant receives a clear outcome of their application.
Important Notice:
ProPharma Group does not accept unsolicited resumes from recruitment agencies or third parties. Please refrain from contacting employees regarding this job posting.
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