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Role & Responsibilities
• Review biomedical literature to identify adverse reaction and non-individual case reports
• Assess reportability, seriousness, and validity of safety cases using regulatory and internal guidelines
• Perform relevancy assessment and ensure accurate identification of reportable safety information
• Conduct narrative review and support MedDRA coding activities
• Provide training and guidance to literature scanner teams on inclusion criteria and case standards
• Collaborate with subject matter experts to maintain physician competency and compliance
• Support quality, consistency, and regulatory adherence in safety case identification
• Perform additional PV responsibilities as assigned by lead or manager
Qualification
• MBBS or MD
Experience
• 0–3 years in Pharmacovigilance / Drug Safety
Skills
• Strong knowledge of PV regulations and regulatory compliance
• Literature case processing and medical review
• Narrative writing and MedDRA coding
• Sound pharmacological and clinical assessment skills
• High attention to detail and strong communication skills
About the Company
Wipro is a leading global information technology, consulting, and business process services company delivering innovative solutions across industries, including life sciences and healthcare. Wipro partners with pharmaceutical organizations worldwide to support drug safety, regulatory compliance, and high-quality healthcare delivery.