Looking for a job

Rose Thomas

@rosethomas1

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I process pharmacovigilance safety cases accurately, supporting timely regulatory reporting and patient safety.

United States

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What I'm looking for

I'm looking for an opportunity in a reputed healthcare organization where I can strengthen my skills and contribute to drug development, research, quality, clinical research, pharmacovigilance, clinical data management, or regulatory affairs.

I've processed serious and non-serious adverse event cases at IQVIA and Accenture, completing triage, duplicate searches, case book-in, data entry, routing, coding, and quality checks.

I'm a Pharm D graduate with clinical internship experience at Amrita Institute of Medical Sciences and hands-on knowledge of ICSR processing, Argus Safety Database, MedDRA, WHODD, clinical research, and ICH-GCP guidelines.

Experience

Work history, roles, and key accomplishments

Pharmacovigilance Service Associate

Accenture

May 2024 - Dec 2024 (7 months)

Performed full data entry of serious adverse event cases in the LSMV database, ensuring accuracy and compliance. Routed cases to appropriate workflows and conducted quality checks.

LSMW Pharmacovigilance Adverse Event Reporting MedDRA WHO Drug Dictionary Data Entry Quality Checks Case Prioritization

Drug Safety Associate Trainee

IQVIA

Jan 2021 - May 2022 (1 year 4 months)

Performed initial assessment, triage, duplicate search, and case book-in in Safety Database Argus 8.1.2. Processed serious and non-serious adverse event cases with accurate data entry and narrative writing.

Oracle Argus Safety Pharmacovigilance Adverse Event Reporting MedDRA WHO Drug Dictionary Data Entry Quality Checks Customer Preparation