Introduzione
The study protocol plays a crucial role in research success, outlining standardized procedures for effective communication among stakeholders.
Unlike clinical trials, real-world evidence studies lack interventions, relying on patient data from routine clinical care.
Developing non-interventional study protocols requires specific considerations to ensure accuracy and relevance.
The aim of the course is to provide an overview of the standards and definitions needed for writing and publishing an observational study protocol.
Module 1: Study Design
- How to write a good research question
- Study Designs: definitions and properties
- Definition of Exposures and Outcomes
- Standards for writing an observational study protocol
Module 2 : Statistical Analysis & Data Dissemination
- Sample size in observational studies
- Indicators used for the observational research
- Confounders
- Workshop
- Standards for publishing an observational study protocol
Roles in Medical Affairs, Clinical Research, Real World Evidence Generation who must generate pre- and post-marketing Real World Evidences to support corporate product development.
Participant experience
Basic knowledge on the definition of Observational Studies, basic knowledge of descriptive statistics
Interactive lessons with a final workshop for study protocol writing.
Docente/i
Lucia Simoni
Lucia oversees and coordinates the activities of Clinical Data Management, Biostatistics and Epidemiology of Real-World Evidence studies with 20+ years of experience.
She is responsible for ensuring the highest possible quality control in recorded clinical data and for developing strategies to optimize such processes.
She joined Medineos in 2001 as biostatistician. Since 2003 she manages the team of Clinical Data Management, Biostatistics and Epidemiology.
She has deep experience in designing observational studies and thanks to her experience she balances the best methodological solutions with study feasibility.
She is author of several scientific publications and lectures both at national and international congresses. Moreover, she is speaker in webinars and training courses on real-world data generation and the methodology of observational studies.
She was member of the Directive Committee of SISMEC (Italian Society of Medical Statistics).
She is expert in the validation process of Patient-Reported Outcomes.
Education: MS degree in Statistics and a PhD in Population Genetics from the University of Bologna. Moreover she completed a 2-year post-doctorate fellowship at University of Geneva.
Online Training – 2 modules
Module 1 | 20 November 2024 from 2:00 pm to 6:00 pm CET
Module 2 | 25 November 2024 from 2:00 pm to 6:00 pm CET
After the registration, you will receive all details about the connection.
The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
Early Bird: € 845,00* (until 30 October 2024)
Ordinary: € 1035,00*
Freelance – Individual – Academy – Public Administration**: € 600,00*
* for Italian companies: +22% VAT
** Early Bird discount not applicable to Freelance – Academy – Public Administration fee
The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Registrati
Mara Claudia Algarotti
Training Manager & MW Operations
Cosa saprai fare dopo il corso
Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.