Helen Taylor
Open to opportunities
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WORK HISTORY
@Open to opportunities
Providing clinical documentation and administrative support while actively seeking new opportunities in clinical research, healthcare, or public sector organizations. Leveraging experience from previous roles to contribute to process improvement, team coordination, and submission readiness.Key Responsibilities:Supported global clinical and regulatory teams with documentation workflows and eTMF quality checksConducted QC reviews and ensured submission-ready documents for CTA and MAA packagesMaintained document repositories using Veeva Vault, SharePoint, and CTMS platformsCoordinated linguistic reviews and tracked document status across multiple studiesDelivered remote training and onboarding materials to support team developmentSelected Successes:Led document QC for a multi-country CTA submission at AstraZeneca, ensuring timely delivery and zero audit findingsDeveloped onboarding guides for new regulatory associates, improving team ramp-up time by 30%Supported system rollout for a new document management platform, training over 50 users across global teamsCollaborated with study delivery teams to prepare documentation for inspection-readiness auditsCurrently open to Clinical Trial Assistant, Documentation Coordinator, or Administrative Support roles—remote or hybrid—within pharma, biotech, CROs, or public sector organizations.
EDUCATION
Liverpool John Moores University
Pg Certificate
Liverpool John Moores University
PGCert Clinical Trials Administration
SKILLS
ABOUT HELEN TAYLOR
I’m an experienced project support and documentation specialist with a strong background…
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