Über Rossana
- Medical strategy, medical plans, and medical leadership
- Global Medical Information (content creation, scientific responses, MI operations)
- KOL engagement & building external expert networks
- Medical education, advisory boards & educational activities
- Review of scientific, clinical operations, promotional & non-promotional materials
- Experience at the diagnostics–pharma interface
- Strong scientific communication skills & ability to translate evidence for diverse audiences
- Fast onboarding, highly reliable execution & strong customer focus
- Winning grant-writing
Italienisch
Muttersprachlich oder zweisprachig
Englisch
Verhandlungssicher
Deutsch
Konversationssicher
Projekt- und Berufserfahrung
- Open Innovation in Life Sciences (OILS) AssociationConference Co-Chair & Associate DirectorOktober 2020 - Oktober 2022 (2 Jahre)Zürich, Switzerland• Led the organization of an international scientific conference, managing a cross-functional team, exceeding fundraising goals, and attracting 200+ participants.• Directed innovative initiatives bridging academia and MedTech, fostering collaboration between academia, Medtech and pharma-industry.
- AbbVieMedical Affairs AssistantJanuar 2025 - Juli 2025 (6 Monate)Cham, SwitzerlandFor the launch of ELAHERE, a novel precision medicine treatment for ovarian cancer:• Developed compliant, scientifically accurate digital medical information for HCPs.• Co-led the organization of a national Advisory Board with pathology KOLs to enable impactful scientific exchange and inform strategic planning for biomarker–diagnostic readiness.• Created structured, compliant Advisory Board meeting minutes, capturing key clinical and strategic insights.
- SFL Regulatory Affairs & Scientific Communication (consultancy firm)Medical Affairs Associate/Medical WriterApril 2022 - Januar 2024 (1 Jahr und 9 Monate)Basel, SwitzerlandTimely delivered documents across multiple therapeutic areas and medical devices, ensuring scientific accuracy, regulatory compliance, and alignment with client expectations:• Authored and managed clinical and lifecycle documents for regulatory submissions (e.g., Clinical Evaluation Reports, Investigator's Brochures, scientific summaries) under ICH and MDR frameworks.• Conducted high-quality systematic literature searches using PubMed and Embase and appraisal.• Drafted accurate publications and perfomed QC of various documents.
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Ausbildung und Abschlüsse
- PhD in2024PhD in
- PhD in MolecularNTNU and UZH2018PhD in Molecular