Feedback

×

Profile Background
ZS

Zoya Syed

ID: CCE384908

Zoya Syed

ID: CCE384908

FollowMessage
Profile Background
ZS

Zoya Syed

ID: CCE384908

    Sponser Title

    About Zoya Syed

    Pharm.D professional with a year of hands-on experience in Pharmacovigilance and Clinical Research at St. Philomena’s Hospital, Bangalore. Skilled in processing over 80 ICSR/ADR cases—including materiovigilance and hemovigilance—through VigiFlow, ensuring full ICH-E2A compliance. Successfully led a 35-patient prospective study with 100% source data verification, documented 8 serious adverse events, and upheld zero protocol deviations. Proficient in MedDRA v26.1 coding with 98% accuracy and certified in ICH GCP E6(R3). Clinical training enhances case narratives, delivering quality beyond standard data entry.

    Employment History

    2024
    SP

    Intern

    1st Nov 2024 to 25th Dec 2025

    See More

    Roles & Responsibility

    Oversee comprehensive pharmacovigilance operations managing 80+ ADR/ICSR cases with full ICH-E2A compliance and timely WHO expedited reporting. Execute precise MedDRA coding and support regulatory submissions and signal detection with 98% accuracy. Apply Naranjo and WHO-UMC algorithms to identify safety signals, ensuring robust aggregate reporting. Conduct quality control on 200+ records to reduce discrepancies by 35%. Lead clinical studies with strict protocol adherence, meticulous data verification, and regulatory documentation. Provide expert medication reviews resolving therapy problems, optimizing treatments, and advancing antimicrobial stewardship, achieving significant medication error reduction and high customer satisfaction.

    Skills

    • Ability to work in a team environment
    • Ability to manage a team and give

    Education

    2025

    PharmD

    Rajiv Gandhi University

    19th Aug 2019 to 25th Dec 2025

    2025

    Doctor of Pharmacy (Pharm.D) — 6-Year Program

    Al Ameen College of Pharmacy, Bangalore

    1st Jan 2019 to 1st Jan 2025

    Expertise

    Drug Information

    0/5

    FDA MedWatch

    0/5

    WHO PV Standards

    0/5

    ALCOA+

    0/5

    EMR/HIS

    0/5

    MS Excel Advanced

    0/5

    CTMS Concepts

    0/5

    Medication Therapy Management

    0/5

    ADR Management

    0/5

    CDSCO

    0/5

    DKA Protocols

    0/5

    Antimicrobial Stewardship

    0/5

    ALCOA+ Principles

    0/5

    Source Document Verification

    0/5

    Data Quality Control

    0/5

    Duplicate Detection

    0/5

    Query Management

    0/5

    Database Maintenance

    0/5

    Regulatory Binders

    0/5

    VigiFlow

    0/5

    MedDRA v26.1

    0/5

    Causality Assessment

    0/5

    Signal Detection

    0/5

    Expedited Reporting

    0/5

    AE/SAE Reporting

    0/5

    CTCAEv5.0

    0/5

    ICF Management

    0/5

    ICSR Processing

    0/5

    ICH-E2A

    0/5

    GCP E6(R2/R3)

    0/5

    E2B(R3)

    0/5

    GVP Module VI

    0/5

    CIOMS

    0/5

    WHODrug Dictionary

    0/5

    EudraVigilance

    0/5

    Sponser Title