
Timeline
About me
PharmD | Central Lab Oversight Manager - Enovalife for GSK
Education

Université de paris
2015 - 2021Doctor of pharmacy - pharmd, industrial course pharmacyThesis June 2022 : « New digital initiatives enhancing patient enrollment in industrial clinical trials : opportunities and challenges analysis »Key words : Recruitment websites, decentralized clinical trials, social media promotion, eConsent, EHR pre-screening.

Université de paris
2015 - 2016Common first year of health studiesRanked 1st out of 2200 for pharmacy

Université de montpellier
2020 - 2021Master’s degree : clinical operations management & data management-Project management : timelines/budget/quality -Clinical trials regulation-Data management-Study feasibility-Protocol writing
Experience

Pharmacie
Jun 2018 - Jul 2019- Dispensed prescribed drugs and pharmaceuticals- Stock management- Advising and assisting patients with medical purchases and product selection
Student employee in Pharmacie Oulie
Sept 2017 - Jul 2019Student employee in Pharmacie de la Prefecture
Jun 2018 - Jul 2018

Ap-hp, assistance publique - hôpitaux de paris
Jun 2019 - Jul 2019Clinical research internshipConducted a study about metformin-associated lactic acidosis to identify the predictive factors of this disease : bibliographic research, data collection & data entry, statistical analysis of a case series.

Ap-hp, assistance publique - hôpitaux de paris
Sept 2019 - Jan 2020Fifth-year pharmacy hospital internshipNeonatal resuscitation department :-Checked prescriptions and biological results-Helped medical interns with prescriptions and assisted them with the clinical examination of premature infants-Daily staff with cliniciansParenteral nutrition department :-Participated in the production and the quality control of parenteral nutrition products meant for premature infants-Validation of prescriptions-Conducted a study about the stability of different parenteral nutrition products components Show less
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Cerc (cardiovascular european research center)
May 2020 - Aug 2020Clinical project leaderCRO specialized in medical device clinical trials in cardiology : Initiation and follow-up of 2 international clinical studies (2 different medical devices) : -Project management, monitoring visits planning, sponsor meetings-Regulatory submissions follow-up-Set-up of Investigator Study File (ISF) and management of eTMF-Co-lead Site Initiation Visits (SIVs) with CRA-Safety activities : Clinical Events Committee (CEC) management, collect of source documents for adverse events adjudication, follow-up of adverse events-Contract with Data and Safety Monitoring Board (DSMB) members-Monitoring visit reports review-Budget follow-up-Writing of study NewslettersTrainings : GCP, Monitoring, Helsinki déclaration & ISO 14155, Clinical research in cardiology Show less

Sanofi
Sept 2020 - Sept 2021Global study managerPhase III program composed of 4 studies (40 countries/+4000 patients) - Multiple Sclerosis, Neurology:-Collaboration set-up and management of 3 service providers related to recruitment :• Recruitment websites : coordinated the set-up, content review, EC submissions and launch of recruitment websites in 5 countries (~100 people involved in the review process) and followed-up online recruitment activity with vendor/local teams/sites.• Pre-screening software : oversight of vendor's activity related to site activation, pre-screening data central analysis.• Recruitment advertising via a patient network : coordinated the creation of 3 webinars and a direct email campaign meant for MS patients to share clinical trials opportunities.-Participated to global recruitment follow-up & strategy + problem solving in COVID-19 context : patient distribution changes, back-up sites activation in close collaboration with Regional Study Managers (RSMs).-Led an animation video project meant for patients : budget/timelines validation, script creation, storyboard review, coordination of the team validation and translations.-Budget management : Global Budget Monitoring (GBM) follow-up, invoices.-Risk management : Study Risk Management Plan (SRMP) review and follow-up-Protocol deviation review and follow-up Show less

Enovalife
Jan 2022 - nowManagement of +20 CMI (cell-mediated immunity) processing laboratories: selection, evaluation, certification, clinical studies set-up/conduct/closure :-Coordination of clinical studies set-up : main point of contact between study team and lab team-Contracts set-up with labs-Budget management -Capacity management-Logistics coordination for turn around time (shipment of samples from sites to labs within 24H after blood draw)-Study conduct follow-up-Follow-up of protocol deviations Show less
Central Lab Oversight Manager for GSK
Oct 2023 - nowLab Study Manager for GSK
Jul 2022 - Oct 2023CMI lab logistics coordinator for GSK
Jan 2022 - Aug 2022
Licenses & Certifications

Toeic : 940/990
Ets globalJul 2020
Permis b
Agence nationale des titres sécurisés - antsJan 2017
Agilepm foundation
Apmg internationalJul 2023
Volunteer Experience
Secretary General
Issued by Association Pharmacie Paris Descartes (PPV) on Sept 2017
Associated with Camille PHELIPOT
Languages
- frFrançais
- anAnglais
- esEspagnol
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