An Young Taylor
Clinical Research Associate @Hôpital Fondation Adolphe de Rothschild
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WORK HISTORY
Clinical Research Associate @Hôpital Fondation Adolphe de Rothschild
Paris, FR
Maintained the Investigator Site File (ISF) to ensure regulatory compliance and audit readiness- Contributed to 6 protocols in pediatric neurosurgery and 4 protocols in adult epilepsy (RIPH1 and RIPH3), supporting site compliance, documentation management, and data integrity- Participated in drafting site Standard Operating Procedures (SOPs) and ensured adherence to ICH-GCP guidelines- Ensured data integrity through accurate entry into Clinfile, RedCap, Ennov V8, and CRFs, and managed queries with CRO monitors- Coordinated communication between CRO teams, patients, and internal departments to support study progress- Utilized Innogec, DxCare, Doctorlib, and Filemaker for patient follow-up and data traceability- Managed clinical trial logistics including patient screening, visit scheduling, and telephone follow-up- Participated in study close-out activities, including the archiving of study documentation in compliance with regulatory requirements.
EDUCATION
Paris-Sud University (Paris XI)
Doctor of Philosophy (Ph.D.), Pharmaceutical Sciences
Universidad de Sonora
Doctor of Philosophy (Ph.D.), Nanotechnology
Universidad de Sonora
Master’s Degree, Nanotechnology
Université Paris Cité
DU Clinical Research Associate , Clinical Research Associate
Universidad de Sonora
Bachelor’s Degree, Medical Laboratory Scientist
SKILLS
ABOUT AN YOUNG TAYLOR
I am a scientist with 8+ years in cancer therapy R&D, now channeling my deep passion for healthcare impact into the core of clinical development. I have recently completed specialized CRA training and am GCP-certified. My transition is driven by the desire to apply my scientific rigor directly to patient-centric research: Dual PhDs (Pharmacy + Materials Science) with a proven ability to translate complex protocols and ensure data integrity: Hands-on knowledge of ICH-GCP, clinical trial lifecycle, monitoring, and patient safety protocols: Expert at identifying discrepancies and proposing solutions—directly applicable to source data verification and query management. & : Fluent in English, French, and Spanish. Thrive in dynamic, global, cross-functional teams: Assistant Clinical Research Associate (Assistant CRA) Clinical Trial Assistant (CTA) Clinical Research Associate - Junior / In-House CRA\'. Are a Clinical Operations Leader or an experienced CRA – I am eager to learn from your insights. Value the rigor and precision that scientists bring to clinical roles. Are building a team passionate about patient safety, data quality, and impactful research.#ClinicalResearch #CRA #AssistantCRA #CTA #EntryLevel #GCP #ICHGCP #Pharma #Biotech #CRO #ScientificTransition
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