





Hybrid remote, mid-level (3 years), and metro Chennai increase applicant density.
Role requires pharmacovigilance-specific systems and terminology (Argus, E2B, MedDRA), limiting cross-industry transferability.
Mandatory 3+ years plus direct Argus experience, MedDRA knowledge, and SQL skills impose high shortlisting strictness.
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Support and maintain Drug Safety applications including Argus and related systems ensuring alignment with business strategy and IT governance.
Generate validated and ad hoc safety data listings and reports for regulatory submissions, audits, and internal customers.
Troubleshoot technical issues in data transmission (E2B) and collaborate with IT and PVSS teams to protect safety data systems and facilitate new software releases.
Bachelor’s Degree in Computer Science or related field.
At least 3 years of IT or direct Drug Safety Systems support experience.
Direct experience with Argus safety database and familiarity with safety data repositories and EDC platforms.
Legal right to work in India (location: Chennai, office or home-based).
Experienced in pharmacovigilance drug safety application support with strong technical troubleshooting and project management skills.
Comfortable working in a fast-paced, high-energy environment handling time-sensitive regulatory and audit requests.
Proficient with safety database structures, reporting tools, SQL/PLSQL, and coding dictionaries like MedDRA and WHODrug.