Laura Domingo Rodriguez
Clinical Lead at iVascular- Claim this Profile
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Inglés Full professional proficiency
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Catalán Native or bilingual proficiency
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Castellano Native or bilingual proficiency
Topline Score
Bio
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Credentials
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Design and Interpretation of Clinical Trials
The Johns Hopkins University at CourseraMay, 2020- Sep, 2024 -
Training Course of Experimental animal for human diseases
PRBB (Barcelona Biomedical Research Park)Jun, 2017- Sep, 2024 -
Write it clearly: fundamentals of good scientific writing.
PRBB (Barcelona Biomedical Research Park)May, 2017- Sep, 2024 -
Good Clinical Practice (GCP)
The National Institute on Drug Abuse (NIDA)May, 2020- Sep, 2024 -
Certificate in Advanced English (C1)
University of Cambridge -
Training Course of User Research Staff for the Use of Animals for Experimentation
Universitat Autònoma de Barcelona
Experience
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iVascular
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Germany
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Medical Equipment Manufacturing
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100 - 200 Employee
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Clinical Lead
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Jun 2022 - Present
- Design, planning and management of first in human and post-marketing clinical follow-up (PMCF) clinical trials of class II a/b and class III endovascular, neuroradiology and cardiovascular Medical Devices. - Preparation and review of clinical documentation (Protocol, ICF, PIS) - Design and management of eCRFs. - Coordination and interaction with CROs and KOLs, as well as leading relevant meetings. - Preparation of reports and plans in accordance with the European Medical Device Regulation (MDR) 2017/745 as the Clinical Evaluation Plan (CEP), Post-Marketing Clinical Follow-up (PMCF) plan and report, Summary of Safety and Clinical Performance (SSCP) and Post-Market Surveillance (PMS) plan. - Systematic review of literature and scientific databases. - Develop all activities in compliance with ICH Good Clinical Practices and under an ethical (ISO 14155, Clinical investigation of medical devices for human subjects) and regulatory frame. Show less
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Vall d’Hebron Institute of Research (VHIR)
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Spain
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Research Services
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1 - 100 Employee
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Clinical Trials Study Coordinator
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Sep 2020 - Jun 2022
- Responsible to manage and coordinate daily clinical trials from phases I-IV, including immunotherapy and medical device. Conducting 10 to 15 simultaneous clinical trials. - Worked with the study team, sponsors, and institutions to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study. - Contribute to the development of a new clinical trial by designing and writing the study protocol and obtaining permissions from the ethics committee. - Report project development, protocol deviations and serious adverse events - Monitoring activities and management of eCRF. - Negotiate contracts and manage payments. - Develop all activities in compliance with GCP and under an ethical and regulatory frame. Show less
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Postdoctoral Researcher - Neurophar Lab
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Mar 2020 - Jun 2020
Managing projects and writing scientific articles.
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PhD Student in Neuroscience - Neurophar Lab
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Jan 2015 - Mar 2020
- Responsible for the development and coordination of scientific projects working in a multidisciplinary team with international collaborators to joint results and fulfil deadlines.- Strategic thinking and creative problem-solving abilities required to face up daily experimental unexpected issues.- Statistical analysis of scientific data obtained in large and complex experiments.- Attendance and presentation of my work to national and international scientific congress acquiring good public scientific abilities.- Preclinical research expertise in neuroscience focused on cognitive behavior and mental health disorders: behavioral, biochemical and molecular techniques. Show less
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Final Master Thesis
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Jan 2015 - Aug 2015
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Universitat autonoma
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Spain
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Higher Education
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700 & Above Employee
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University Teacher
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Jul 2017 - Jul 2019
- Public speaking abilities and teaching to students in English. - Organization skills obtained preparing lectures content and class dynamics. - Public speaking abilities and teaching to students in English. - Organization skills obtained preparing lectures content and class dynamics.
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Intership at Myogenesis, Inflammation and Muscle Function group
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Sep 2013 - Sep 2013
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Education
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Universitat Pompeu Fabra - Barcelona
PhD in Biomedicine, Excellent Cum Laude -
INESEM Business School
Master in Clinical Trial Monitoring and Pharmaceutical Development -
Universitat de Barcelona
Master's degree, Neuroscience -
Universitat Pompeu Fabra
Bachellor's degree, Biomedicine and Human Biology -
Escola del Sol
Curs de monitor d'activitats de lleure infantil i juvenil -
Vall d'Hebron Institut de Recerca (VHIR)
Clinical Trial Assistant (CTA) Course - Regulatory Affairs