
Marzia Rizzo
@marziarizzo
I coordinate clinical research projects, documentation, and quality-focused study operations.
What I'm looking for
I'm applying my genetics, biotechnology, and clinical drug development background to clinical trial oversight and study operations.
At Stockholm University and SciLifeLab, I led research projects and study activities across multidisciplinary teams, coordinating timelines, priorities, deliverables, and issue resolution with academic, industry, and international collaborators.
My PhD research at the University of Kent took a multi-year genetics project from experimental design through data analysis, publication, and international presentations. I also prepared and reviewed scientific and technical documentation with close attention to accuracy, consistency, and data quality.
At CarryGenes AB, I supported quality and compliance through QC protocols, study reports, SOP-related documentation, and review of research data. My Clinical Drug Development training covers Phase I-IV trials, ICH-GCP, CRF design, eTMF, safety reporting, pharmacovigilance, and clinical study documentation.
Experience
Work history, roles, and key accomplishments
Postdoctoral Researcher
Stockholm University
Mar 2024 - Dec 2025 (1 year 9 months)
Led and managed research projects and study activities across multidisciplinary teams, coordinating timelines, priorities, and deliverables. Identified and resolved operational and scientific problems during study execution and mentored junior researchers.
Workshop Organizer & Council Member
Stockholm University & SciLifeLab
Mar 2024 - Aug 2025 (1 year 5 months)
Designed and delivered in-person and online workshop events, including scientific and career development, handling communication and materials. Maintained the SciLifeLab website, creating engaging content including news updates, training events, and outreach materials.
Doctoral Researcher
University of Kent
Sep 2018 - Jul 2023 (4 years 10 months)
Led a multi-year genetics research project from experimental design through data analysis, publication, and presentation. Coordinated international collaborations and managed project timelines, resources, and competing priorities.
Scientist - Technical Documentation & Compliance
CarryGenes AB
Apr 2022 - Dec 2022 (8 months)
Worked in a biotechnology environment applying GLP and QMS principles to research activities and documentation. Prepared QC protocols, study reports, and SOP-related documentation, supporting data integrity and traceability.
Education
Degrees, certifications, and relevant coursework
Uppsala University
Clinical Drug Development Programme, Clinical Drug Development
2025 -
Training in Phase I-IV clinical trials, study design, ICH-GCP, and clinical study documentation.
Stockholm
Regulatory Affairs & GDP Training, Regulatory Affairs & GDP
2026 - 2026
Training on EU regulatory requirements for Marketing Authorisation Applications and GDP compliance.
University of Kent
Doctor of Philosophy, Genetics
2018 - 2023
Doctoral research in genetics focusing on microbiology, infectious diseases, and molecular biology.
Stockholm University
Master of Science, Cancer and Human Viruses
Master of Science with focus on cancer and human viruses (HPV).
University of Messina
Bachelor of Science, General Biology
Bachelor of Science with focus on general biology.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Salary expectations
Job categories
Skills
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