VTAbout Veronia
With over a decade of experience managing global clinical programs and regulatory strategies, I help pharmaceutical and biotech companies accelerate their studies, secure approvals, and optimize vendor performance.
My dual expertise in Clinical Trial Management (Phases I–IV) and Regulatory Affairs (EMA/FDA submissions, compliance, inspections) allows me to bridge science, operations, and regulations to deliver results in high-stakes environments.
- Proven track record in oncology, hematology, and rare diseases
- Leadership in vendor negotiations (CROs, labs) and budget optimization
- Strong knowledge of ICH-GCP, EMA, FDA and international regulatory frameworks
- Experienced in rescuing delayed studies and aligning global stakeholders
If you’re looking for a hands-on senior consultant to drive your trial forward, solve complex regulatory challenges, or secure operational excellence, let’s connect.
English
Native or bilingual
French
Native or bilingual
Remote only
Primarily works remotely
Experience
- Innate PharmaSenior Clinical Trial Manager andRegulatory affairs managerBIOTECHJuly 2024 - Today (1 year and 11 months)Marseille, FranceInternational Phase II Oncology Trial with AstraZeneca• Reduced study timeline by 1 year through strategic protocol amendments• Led full-service CRO oversight (budget, milestones, quality delivery)• Directed site and country selection, activation, and recruitment strategies• Oversaw interim analyses: delivered TFLs 1 week early, improving communication and decision-making• Drafted protocol and coordinated IND submission within 1 month• Authored abstracts and posters for scientific congresses• Took on additional responsibilities as Regulatory Affairs Manager
- Acticor BiotechClinical Trial ManagerBIOTECHSeptember 2022 - June 2024 (1 year and 9 months)Paris, FranceInternational Phase II Trial Acute Ischemic Stroke• Managed cross-functional team (Regulatory, QA, CRA, DM) to accelerate timelines by 2 weeks• Developed interactive dashboard to enhance data transparency and CRO performance• Increased patient recruitment by 20% through targeted site engagement strategies• Improved eTMF (Veeva Vault) quality, resulting in successful inspections by 4 health authorities (Germany, Czech Republic, France)• Led site training workshops, cutting data discrepancies by 50%
- Covance (Dedicated to MSD)Clinical Trial ManagerPHARMACEUTICALS INDUSTRYJune 2020 - April 2022 (1 year and 10 months)Paris, FrancePhase II–III Trials Digestive Solid Tumors- Cross-functional management of Team on 3 Project- CTMS Management metrics- Publication strategic decision- Budget Management- FDA/EMA Project Management- Roadmap and MS Project Management- Stategic communication to leadership Team- Training, mentor, evaluate CRA
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Education
- Good Clinical Practice Certificate (Refresher)MSD2021Good Clinical Practice Certificate (Refresher)
- CTMS Training CertificateLYSARC2017CTMS Training Certificate