Description

Why work with me?

I am a pharmaceutical project and program management consultant, bringing both operational and strategic expertise built over more than 10 years in the pharma and biotech industry. I have led cross-functional assignments in regulatory affairs, clinical operations, quality, market access, and digital deployment across France and Europe. Bilingual in French and English, I support international projects covering diverse portfolios in OTC, oncology, and cosmetics.

I first gained technical expertise as a QC Biochemist at GlaxoSmithKline (France), then as a Clinical Project Manager at Johnson & Johnson (France). I went on to take roles in regulatory coordination and compliance at Pfizer (UK) and Pharmalex (Cencora, Germany), where I managed multiple outsourcing projects and programs with cross-functional teams of up to 20 people—covering budget definition/management, KPIs, and close-out. At Bristol Myers Squibb (France), I ensured the rollout and follow-up of digital oncology tools to improve patient care, while guaranteeing full legal and regulatory compliance.

The common thread throughout my career: acting as a bridge between science, operations, and external partners, ensuring compliance across portfolios and processes.

How I can help you?

Program/Project Management : steering clinical, regulatory, or quality projects; planning, budgeting, and vendor coordination.
Vendor Management : CRO/CMO selection and oversight, KPI implementation, document audit management, GxP compliance.
Digital Rollout & Training : deployment of digital tools (ERP, Veeva, SharePoint), user training, change management, and design of dedicated training campaigns.

Industry field of expertise

Languages

English
Native or bilingual
French
Native or bilingual

Workplace preferences

Can work on-site

Brussels (up to 50km)

Bristol Myers Squibb UK
Market Access & Public Health - Project manager
PHARMACEUTICALS INDUSTRY
September 2024 - August 2025 (11 months)
Rueil-Malmaison, France
Clinical project support (non-interventional trial): coordinated between public institutions (FIAC) and private vendors/CROs to select, activate, and monitor trial sites. Ensured timelines and compliance for study launch.
Contract drafting & negotiation: drafted and refined contracts to clarify scope, deliverables, and data protection. Aligned legal and procurement terms across vendors, scientific committees, and investigator sites.
Stakeholder alignment: acted as liaison between legal, procurement, and scientific stakeholders, ensuring contract terms matched institutional policies and regulatory requirements.
Consensus building & project initiation: facilitated structured discussions to balance scientific objectives with operational constraints, leading to successful study approval and initiation.
market access public health non investigational studies e-oncology
Cencora (PharmaLex)
Program Coordinator
PHARMACEUTICALS INDUSTRY
January 2017 - July 2024 (7 years and 6 months)
Mannheim, Germany
Project governance & execution : built and executed roadmaps, implementation plans, and reporting frameworks (meeting minutes, status reports, KPIs) to keep programs on track.
Team leadership in matrix setups : led and mentored cross-functional project teams (up to 20 people), ensuring alignment and high performance across regulatory, clinical, and operations.
Vendor management & onboarding : selected, onboarded, and trained vendors, maintaining performance through structured oversight and clear communication.
Contract & budget oversight : reviewed SOWs/PSAs, supported invoicing, and monitored project profitability via ERP (Microsoft Dynamics 365).
Cross-functional delivery : coordinated outsourcing programs (regulatory submissions, NDA planning, end-to-end local outsourcing) to achieve client and business objectives.
SOP vendor risk management cross-functional coordination governance & reporting RfP/MSA/SLA/PSA/bid defense
Pfizer
Project coordinator (QA)
PHARMACEUTICALS INDUSTRY
October 2015 - December 2016 (1 year and 3 months)
London, United Kingdom
Data migration & compliance monitoring : analyzed and tracked MAA data migration into a new eDMS system, ensuring accuracy and completeness during system launch.
Training & onboarding : designed communication plans and educational materials, training global and regional regulatory teams on compliant data entry.
Change management support : supported adoption of new digital processes, improving data quality and compliance across multiple regions.
project coordination compliance training & onboarding quality control (QA)