À propos de Sarra
I help organisations advance cancer research by making science tangible, measurable, and impactful.
As a Medical Oncologist with 6+ years of experience spanning R&D and clinical development, I translate complex scientific challenges into concrete strategies — from Phase II & III trial design to evidence generation and scientific communication.
What defines my profile:
🔬 Scientific Impact 20+ peer-reviewed publications in top-tier oncology journals — New England Journal of Medicine, JAMA, Nature Communications, Journal of Clinical Oncology, and more — contributing to research that has directly shaped clinical practice and standards of care.
🤖 Technology & Innovation I actively integrate AI-assisted research, literature review, and data interpretation into my daily practice. I believe that staying ahead of the science means embracing the tools that accelerate it — including prompt engineering and digital health solutions.
🌍 Multilingual Communication Fluent in French, Arabic, and English, with intermediate Dutch — enabling me to engage effectively with international teams, global KOLs, and diverse patient communities across Europe, the Middle East, and beyond.
💊 Clinical & Research Expertise End-to-end leadership of Phase II & III oncology trials · Protocol development · Patient safety oversight · KOL & patient advocacy engagement · Cross-functional collaboration · Grant writing .
🎯 My Strength Building bridges between clinical expertise, rigorous evidence, and cross-functional teams — to generate insights that inform decisions, empower clinicians, and improve patient outcomes.
Get in touch by sending an email to:
Anglais
Bilingue ou natif
Français
Bilingue ou natif
Arabe
Bilingue ou natif
Néerlandais
Notions
En télétravail uniquement
Travaille majoritairement à distance
Expériences
- Breast International Group (BIG-HQ)Medical Advisor & Senior Medical Advisorjanvier 2020 - mai 2026 (6 ans et 4 mois)Belgium• • Led full lifecycle of phase II&III clinical trials and research programs, encompassing protocol development, regulatory documentation (ICFs, CRFs, IBs, CSRs), patient safety oversight, and cross-functional collaboration with academic and pharma partners.• • Drove scientific communication and stakeholder engagement through abstracts, manuscripts, international presentations, press releases, and social media, while representing the association as speaker at international workshops and engaging with patient advocacy groups.• • Contributed to organisational leadership and growth by serving as voting member in Steering Committees, participating in IDMC and advisory meetings, developing grant applications securing €10M in funding, and mentoring staff members.
- Institut Curie (centre de lutte contre le cancer).Fellow in Oncogeneticsmars 2014 - mars 2014Paris, FranceOncogenetics consultation : hereditary tumors, Family consultationOncogenetics Laboratory : genome sequencing, biomarkers
- University Hospital OranResidency in Medical Oncologyseptembre 2008 - novembre 2012 (4 ans et 2 mois)Oran, AlgérieCare of patients with solid tumors, preparation of conferences and local symposia, local and regional presentations
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Formations
- Doctor of Medicine (MD)Faculty of Medicine2008Doctor of Medicine (MD)
- Master's in Medical Oncology (MSc)Faculty of Medicine2013Master's in Medical Oncology (MSc)
Certifications
- Clinical Trial Statistics for Non-StatisticiansEORTC2022
- Designing Clinical Research protocolsECCRT2023