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Aggregate Reporting Specialist PV @ Clin Biosciences

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 Aggregate Reporting Specialist PV

Job Description

    Roles and Responsibilities for PV AI Validation Analyst (UAE)

      • Automate generation of aggregate safety reports using tools like SAS, Spotfire, Python, Power BI, or QlikView.

      • Extract data from safety databases (Argus, ArisG, Veeva Vault Safety, Oracle Clinical) into validated formats.

      • Maintain traceability, version control, and audit readiness for automated outputs.

      • Build data visualization dashboards for safety metrics & compliance monitoring.

      • Collaborate with pharmacovigilance teams to interpret data outputs and ensure regulatory accuracy.

      • Apply scripting, macros, or API-based automation to improve report turnaround time.

      • Ensure alignment with ICH E2E / EMA / FDA aggregate reporting regulations.

    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: hidden_mobile/ hidden_mobile

     

Employement Category:

Employement Type: Full time
Industry: Pharma / Biotech
Role Category: Pharmacist / Medical Representative
Functional Area: Not Specified
Role/Responsibilies: Aggregate Reporting Specialist PV

Contact Details:

Company: Clin Biosciences
Location(s): Bengaluru

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Keyskills:   icsr processing argus meddra coding drug safety pharmacovigilance

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