Local Case Intake Advisor – Pharmacovigilance
Brief Summary:
Candidates with strong expertise in safety case management, regulatory compliance, stakeholder coordination, and pharmacovigilance systems are encouraged to apply.
Job Description:
π WEβRE HIRING | LOCAL CASE INTAKE ADVISOR β PHARMACOVIGILANCE | ASTRAZENECA
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π Location: Bangalore, Karnataka, India
πΌ Position: Local Case Intake Advisor β Pharmacovigilance
π’ Company: AstraZeneca
π Employment Type: Full-Time
π¨βπΌ Experience: 2β5 Years
β‘ Immediate Joiners Preferred
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Educational Qualifications
π Eligible Candidates:
β’ B.Pharm
β’ M.Pharm
β’ PharmD
β’ B.Sc Life Sciences
β’ M.Sc Life Sciences
β’ Biotechnology Graduates
β’ Medical Sciences Graduates
β’ Other Relevant Life Science Disciplines
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Key Responsibilities
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Manage ICSR processing and end-to-end case management activities
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Handle adverse event reporting in accordance with global regulations
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Support pharmacovigilance compliance and Good Pharmacovigilance Practices (GVP)
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Conduct safety data review and medical assessment activities
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Assist with health authority query management and responses
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Perform reconciliation activities to ensure data accuracy
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Support audit readiness and regulatory inspections
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Contribute to Quality Management System (QMS) activities
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Collaborate with internal stakeholders, clients, and vendors
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Ensure compliance with global drug safety and pharmacovigilance requirements
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Required Skills
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Why Apply?
π Opportunity to work on global drug safety programs
π Enhance expertise in adverse event reporting and ICSR management
π Gain exposure to regulatory compliance, audits, and inspections
π€ Work closely with cross-functional teams and global stakeholders
π‘ Strengthen your career in Pharmacovigilance and Drug Safety
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π© Apply Now
π§ Email: mayuri.k@twsol.com
π Email Subject: Local Case Intake Advisor β Bangalore
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Interested candidates are encouraged to apply at the earliest as immediate joiners are being prioritized.
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π Apply via: https://jobportalconnect.com/
Your Gateway to the Best Job Opportunitie
Required Skills:
β Pharmacovigilance (PV)
β ICSR Processing
β Adverse Event Reporting
β Drug Safety Operations
β Good Pharmacovigilance Practices (GVP)
β Regulatory Compliance
β Safety Database Management
β Case Intake Management
β Medical Review Support
β Strong Written and Verbal Communication Skills
β Stakeholder Management
Key Responsibilities:
β Manage ICSR processing and end-to-end case management activities
How to Apply / Contact Info
To apply for this position or make inquiries, please reach out directly to the employer at the contact email address below: