In this webinar, attendees will get to learn how Cevaxin, one of Panama’s top clinical research site networks, removed internal silos and transformed decision-making with real-time dashboards and unified data systems.
The expert speaker will explore their path to complete transparency, including how their use of TRIAL360 facilitated smooth collaboration, improved protocol adherence and access to real-time key performance indicators (KPIs) for human resources (HR), quality assurance (QA), finance, principal investigators (PIs), vendors and sponsors.
The key topics of discussion will include:
- Hidden costs of disconnected data in clinical operations
- Cultural shift required unifying processes across departments
- How real-time dashboards can enhance sponsor trust and trial performance
- Lessons learned and actionable insights applicable to sites or organizations
Register for this webinar today to discover how clinical operations can be streamlined, data silos can be reduced and trial performance can be enhanced using unified systems and real-time dashboards.
Speakers
Hector Gonzalez, Operations Director, Cevaxin
Hector Gonzalez is a Chemical Engineer with more than 15 years of experience directing and executing vaccine clinical trials in the pharmaceutical industry, CROs and research centers. He has experience leading teams focused on process improvement, information technology and data analysis. He currently serves as Director of Operations at Cevaxin, a leading vaccine research center based in Panama.
Message Presenter
Rodrigo DeAntonio, MD, MSc, DrPH, Scientific & Executive Director, Cevaxin
A Medical doctor and Epidemiologist graduated from the Colegio Mayor de Nuestra Señora del Rosario University in Colombia. He earned his Master’s degree in Pharmacoeconomics from Pompeu Fabra University in Spain and his PhD in Public Health from the National Institute of Public Health in Mexico. He received training in cancer epidemiology from the International Agency for Research on Cancer (IARC) in Lyon, France.
He has held various positions in the pharmaceutical industry, focused on clinical research, epidemiology and health economics for Latin America, Asia and Africa. His work has primarily focused on vaccine-preventable diseases, such as rotavirus, pneumococcus, meningococcus, norovirus, HPV, pertussis, hepatitis, respiratory syncytial virus, influenza, chickenpox and dengue.
Since 2018, he has served as Executive and Scientific Director of Cevaxin in Panama conducting clinical and epidemiological studies on vaccine-preventable diseases, medications and medical devices for other diseases. He is an active member of several professional organizations, including SLIPE and APANAC, and is a founding member of SOEPIMO. He has contributed to more than 80 peer-reviewed scientific publications and posters presented at international conferences.
Message PresenterWho Should Attend?
This webinar will appeal to those working in the following areas or having the following job titles:
- Clinical Research Site Executives and Managers
- Clinical Operations Professionals
- Principal Investigators (PIs) and Sub-Investigators
- Quality Assurance (QA) and Compliance Officers
What You Will Learn
Attendees will learn about:
- How decision-making is enhanced by removing data silos
- Real-time visibility’s effects on sponsor trust and protocol adherence
- True obstacles to cross-functional process alignment and how to get past them to create a data-driven, high-performing research culture
Xtalks Partner
Integra IT
At Integra IT, we’re on a mission to expand clinical research possibilities worldwide, especially in diversity, inclusion, and emerging countries. Our comprehensive software ecosystem is cost-convenient and high-efficient for all clinical research stakeholders.
Integra IT’s fully flexible and scalable tech solutions and services enable clinical trials end-to-end control and visibility. Thanks to our software agile engineering and clinical operations expertise, we can streamline clinical trials and make deployments in record time.
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