Looking for a job

Anniechan yeah

@anniechanyeah

Clinical Research Associate at Axella Research who supports oncology trials through risk-based monitoring and clinical data quality checks.

France

Message

What I'm looking for

I’m motivated to contribute to the development of innovative treatments by ensuring clinical trial quality, data integrity, and adherence to regulatory standards. I’m open to roles across France and Europe, including remote work and roles requiring travel.

At Axella Research, I conducted risk-based remote monitoring for a Phase II–III oncology trial, reviewing eCRF data and flagging discrepancies and potential protocol risks. Regular data checks and document reconciliation helped maintain query rates below 5% and eTMF/TMF completeness at 90%, with zero major audit findings reported.

At Sanofi, I conducted a systematic literature review and meta-analysis of approximately 950 studies on COVID-19 vaccine booster reactogenicity. I also analyzed surveillance information and epidemiological datasets, contributing evidence for vaccine research and development.

At Clinitude Inc., I supported Phase II–IV trials across oncology, vaccines, and medical devices, including site initiation, monitoring, and close-out visits. My work on feasibility assessments and study start-up contributed to an 80% improvement in site activation timelines; I also supported enrollment, protocol compliance, and study documentation.

Experience

Work history, roles, and key accomplishments

Clinical Research Associate

Axella Research

Jan 2023 - Sep 2026 (3 years 8 months)

Conducted risk-based remote monitoring of a Phase II-III oncology trial, reviewing eCRF data to identify discrepancies and flag protocol compliance risks. Maintained query rates below 5% and eTMF/TMF completeness at 90% with zero major audit findings.

Risk Based Monitoring Source Documentation Verification (SDV)Electronic Data Capture ETMF TMF Clinical Trial Monitoring ICH GCP Regulatory Compliance Data Quality Oncology

Global Medical Evidence Generation Intern

Sanofi

Feb 2025 - Aug 2025 (6 months)

Conducted systematic literature review and meta-analysis of approximately 950 studies on COVID-19 vaccine booster reactogenicity. Analyzed epidemiological datasets and translated findings into accessible insights for vaccine R&D.

Systematic Literature Review Meta Analysis Data Visualization Epidemiology Medical Affairs HEOR Data Science Covid 19 Vaccines

Clinical Research Associate

Clinitude Inc.

Apr 2021 - Feb 2023 (1 year 10 months)

Supported Phase II-IV clinical trials in oncology, vaccines, and medical devices, conducting site initiation, monitoring, and close-out visits. Improved site activation timelines by 80% and reduced protocol deviations by 85% through CAPA implementation.

Clinical Trial Monitoring Site management Site Start Up ICH GCP Source Documentation Verification (SDV)EDC CAPA Protocol Compliance Oncology Vaccines Medical Devices

Pharmacist

Ministry of Health

Jun 2014 - Aug 2020 (6 years 2 months)

Managed pharmacy operations, ensuring safe dispensing, inventory control, and regulatory compliance. Provided patient counseling and supported pharmacovigilance and community health initiatives.

Pharmacy Operations Dispensing Inventory Control Regulatory Compliance Patient Counseling Pharmacovigilance Medical Terminology

Production Analyst

IMS Health

Mar 2013 - Jun 2014 (1 year 3 months)

Applied MedDRA coding to adverse events and medical terms, and used WHO Drug Dictionary for medication coding. Identified and resolved coding discrepancies through systematic quality checks.

MedDRA Coding WHO Drug Dictionary Pharmacovigilance Data Quality Coding Standards Safety Data Analysis