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About role & responsibilities
• Work in Life Sciences R&D vertical supporting global pharmacovigilance operations
• Create and manage ICSR case identification, data entry, MedDRA coding, case processing, submission and follow-ups
• Monitor and assess safety of pharmaceutical products across clinical and post-marketing stages
• Ensure compliance with global regulatory requirements and client guidelines
• Analyse moderately complex safety data and develop appropriate solutions
• Support detection, evaluation and prevention of adverse drug reactions
• Manage small teams or work efforts when assigned
• Collaborate with internal and client stakeholders
• Work in rotational shifts as required
Qualification
• Bachelor of Pharmacy
• Master of Pharmacy
• MBBS
Skills
• Pharmacovigilance operations and ICSR processing
• MedDRA coding and safety database management
• Regulatory compliance knowledge
• Analytical and problem-solving ability
• Strong documentation and communication skills
Experience
• 7 to 11 years of experience in Pharmacovigilance / Drug Safety
Salary
• Salary Competitive (as per company standards)
Benefits
• Exposure to global life sciences and pharmacovigilance projects
• Career growth and leadership opportunities
• Professional and collaborative work environment
About the company
• Accenture is a global professional services company with strong capabilities in digital, cloud and security
• Provides strategy, consulting, technology and operations services across 120+ countries
• Serves global biopharma clients through advanced technology and intelligent operations centers