Aggregate Reporting Specialist PV CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 0 - 0 years required
Pay: INR 500000 - INR 800000 /year
Type: Full Time
Location: Bangalore
Skills: icsr processing, Argus, meddra coding, drug safety, Pharmacovigilance, automation in pv, pv tech validation, ai in pharmacovigilance
About CLIN BIOSCIENCES
Job Description
Roles and Responsibilities for PV AI Validation Analyst (UAE)
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Automate generation of aggregate safety reports using tools like SAS, Spotfire, Python, Power BI, or QlikView.
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Extract data from safety databases (Argus, ArisG, Veeva Vault Safety, Oracle Clinical) into validated formats.
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Maintain traceability, version control, and audit readiness for automated outputs.
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Build data visualization dashboards for safety metrics & compliance monitoring.
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Collaborate with pharmacovigilance teams to interpret data outputs and ensure regulatory accuracy.
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Apply scripting, macros, or API-based automation to improve report turnaround time.
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Ensure alignment with ICH E2E / EMA / FDA aggregate reporting regulations.
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Qualifications PV AI Validation Analyst (UAE)
- B.Pharm / M.Pharm / Pharm.D or M.Sc in Life Sciences / Biotechnology / Pharmacology
- Knowledge of pharmacovigilance processes (ICSR, MedDRA, WHO-DD, E2B)
- Familiarity with certain tools or automation in drug safety systems (e.g., Argus, VigiBase)
- Bonus: Skills in Python, SQL, Power BI or exposure to RPA/NLP platforms
Interested to apply can share CV or call/WhatsApp to Hr Reenu
Contact information: 9342735755/ 9384592766