Adeline Bourgoin

Adeline Bourgoin has a comprehensive work experience in the field of clinical research and data management. Adeline started their career in 2007 as a Clinical Trial Pharmacist Associate at the University Hospital Nancy, where they managed various phase I-III clinical trials in different therapeutic areas. Adeline also worked as a Quality Assurance Officer and Clinical Research Coordinator, overseeing study set up, running, and end in clinical trials.

Adeline then joined Servier as a Clinical Research Associate, where they conducted co-monitoring visits and ensured compliance with ICH GCP, SOPs, and regulatory requirements. Adeline also served as a Quality Assurance Officer during their time at Servier, conducting audits of designated study centers, preparing staff for inspections, and ensuring adherence to SOPs.

In 2013, Adeline joined Retroscreen Virology as a Clinical Research Associate/Quality Control Manager. Adeline'sresponsibilities included overseeing project-related QC activities, coordinating with staff and external stakeholders, and ensuring project timelines and compliance.

Adeline later joined hVIVO as a Project Data Manager and CRA. Adeline coordinated and acted as the point of contact for data management activities in multiple studies, participated in meetings, and led data management in various phase 1 and 2b studies.

Most recently, Adeline joined Syneos Health (Previously INC Research/inVentiv Health) as a CRA II, where they are currently employed.

Adeline Bourgoin obtained their Doctor of Pharmacy - PharmD degree from the University of Pharmacy, Tours (France) between 2000 and 2007. Adeline then pursued a Research Doctorate in Clinical Research Coordination from the University of Pharmacy, Nancy (France) from 2007 to 2012.