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Role & Responsibilities
• Review published biomedical literature for identification of adverse reaction case reports and non-individual case reports
• Apply regulatory and internal guidance to determine case validity and reportability
• Perform relevancy assessment based on accepted pharmacovigilance guidelines
• Provide training and guidance to literature scanners on inclusion criteria
• Collaborate with subject matter experts to ensure team capability and compliance
• Perform additional pharmacovigilance tasks as assigned by lead or manager
Qualification
• MBBS or MD
Experience
• 0–3 years of experience in Pharmacovigilance / Drug Safety
Skills
• Strong knowledge of global PV regulatory guidelines
• Narrative writing and medical case assessment
• MedDRA coding proficiency
• Understanding of pharmacological concepts
About the Company
Wipro is a leading global information technology, consulting, and business process services company that delivers innovation-led solutions to clients across industries, including life sciences and healthcare. With a strong presence worldwide, Wipro supports pharmaceutical organizations in ensuring drug safety, regulatory compliance, and patient-centric healthcare delivery.
Interested candidates can share their resumes at varsha.kamalapurkar@wipro.com