Pharmacovigilance Services New Associate

Roles & Responsibilities
• Create and manage ICSR case identification and data entry
• Perform MedDRA coding and case processing activities
• Ensure accurate entry of safety data into pharmacovigilance databases
• Handle case submissions in compliance with regulatory requirements
• Conduct follow-ups for incomplete or pending safety cases
• Work in alignment with global pharmacovigilance guidelines and SOPs
• Process routine drug safety cases as per defined procedures
• Collaborate within the pharmacovigilance team and report to supervisor
• Support drug safety surveillance and regulatory adherence initiatives

Qualification
• MSc (Life Sciences) / B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)

Experience
• 0–1 year experience in Pharmacovigilance
• Freshers eligible

Skills
• Basic understanding of Adverse Event (AE) reporting
• Knowledge of ICSR lifecycle and case processing
• Familiarity with MedDRA terminology
• Awareness of drug safety database concepts
• Strong attention to detail and data accuracy
• Ability to work in rotational shifts
• Good written and verbal communication skills
• Team-oriented and compliance-focused mindset

About the Organization
Accenture is a global professional services company providing consulting, technology, and operations services, including pharmacovigilance and drug safety support to leading pharmaceutical and healthcare organizations worldwide.