Florence Renard
Loverval
Profil professionnel
Senior Clinical Project Manager with extensive experience in clinical research, including 7+ years in biotech and multidisciplinary team coordination. Brings over 20 years of expertise in project management, communication, leadership, and healthcare professional engagement.
Proven ability to develop and deliver scientific and clinical content, support education activities, and collaborate cross-functionally with medical, commercial and field teams.
Currently strengthening expertise in diabetes care and digital health technologies (insulin therapy, continuous glucose monitoring and insulin pump systems) to support clinical excellence and patient-centered education.
Therapeutic experience includes oncology/hematology, immunology, neurology, vaccines, infectious diseases, paediatrics, rheumatology, dermatology, and rare diseases.
Key strengths: proactive, organized, self-starter, flexible, and team-oriented. Strong leadership in CRO oversight, inspection readiness, SOP development, risk management, and complex multinational trials.
Certified in GCP, FDA regulations, and Artificial Intelligence.
Vue d'ensemble
19
19
years of professional experience
3
3
years of post-secondary education
Expérience
Clinical Trial Manager
argenx
Ghent
2024.02 - Current
- Responsible for a worldwide non interventional trial in MMN disease, 410 participants in Europe, APAC, US and Canada
- Gathered and reviewed study data.
Senior Clinical Project Manager
PDC Line Pharma SA
Liège
2020.06 - 2025.08
- Managed a Phase I NSCLC gene vaccine study (Belgium, Netherlands, France, Germany, Poland): budget control, study plans, site/vendor selection, team coordination, KPI tracking, DSMB prep, eCRF review, data analysis and SOP development to ensure GCP inspection readiness.
Clinical Project Manager
Celyad SA
2018.04 - 2020.06
- Managed three Phase I CAR-T colorectal cancer studies (Belgium & UK): budget control, study plans, vendor oversight, team coordination, data review and site payment tracking.
Clinical Project Manager/Lead CRA/CTL
Freelance
2011.01 - 2018.04
- Managed and monitored Phase I-IV trials across oncology, gastroenterology, infectious diseases, HIV, RA, respiratory, systemic sclerosis, hematology, pediatric neurology, and medical devices in Europe and globally.
- Expertise includes: End-to-end study management (start-up to close-out), Budget control, vendor/site oversight, team leadership, Regulatory submissions, contract negotiations, SOP development, Risk-based monitoring and GCP, engaging and motivating global investigational sites, identifying enrollment and operational barriers, strengthening investigator relationships when recruitment or quality issues were identified
Clinical Project Manager
Schering Plough/MSD Belgium
2007.01 - 2011.04
- Managed Phase II-IV studies across gastroenterology, rheumatology, infectious diseases, infertility, vaccines, dermatology, and hepatology.
- Responsibilities: feasibility, budget tracking, site/vendor oversight, CRA training, document review, risk-based monitoring, SOP writing, and mentoring.
Formation
Diploma in Nutrition -
Diploma of assistant to Management -
1993.01 - 1994.01
Bachelor - translation
1991.01 - 1993.01
Compétences
- Very good communication skills
- Organized
- Pro-active
- Self-starter
- Team player
- Flexible
Language
French
Bilingual
English
Bilingual
Dutch
Bilingual
German
Intermediate
Italian
Intermediate
Additional trainings
- Certificate in Artificial Intelligence, 2025-05-01
- Online training in Diabetes Management (2026 – ongoing)
Informations complémentaires
- Tennis, padel, pickleball
- Jogging
- Reading
Chronologie
Clinical Trial Manager
argenx
2024.02 - Current
Senior Clinical Project Manager
PDC Line Pharma SA
2020.06 - 2025.08
Clinical Project Manager
Celyad SA
2018.04 - 2020.06
Clinical Project Manager/Lead CRA/CTL
Freelance
2011.01 - 2018.04
Clinical Project Manager
Schering Plough/MSD Belgium
2007.01 - 2011.04
Diploma of assistant to Management -
1993.01 - 1994.01
Bachelor - translation
1991.01 - 1993.01