Shannon Roznoski, CCDM, CCRP
Director of Product Management, Advarra
Shannon Roznoski is the Director of Product Management at Advarra. Roznoski guides the strategic planning and management of clinical data management solutions at Advarra. She is an advocate for the adoption of industry standards to ensure Advarra solutions meet the needs of its customer community. Roznoski has over 20 years of clinical data management and IT experience, and is a Certified Clinical Data Manager (CCDM) through the Society for Clinical Data Management (SCDM).
Latest Posts by Shannon
Beginner’s Guide to 21 CFR Part 11 Compliance
FDA released regulations in 1997 outlining how 21 CFR Part 11 applies to electronic records and electronic signatures in clinical research.
Q&A – Regulatory Fine Points: Exploring 21 CFR Part 11 Validation
Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.
Regulatory Fine Points: Exploring 21 CFR Part 11 Validation
FDA is placing an increased emphasis on compliance with 21 CFR Part 11. Institutions, health systems, IRB offices, private research clinics, and developers—to name a few—need to understand the basics of the regulation and how to comply.
Tips for Writing Effective Edit Checks in eCRFs
Learn how to write effective edit checks in electronic case report forms (eCRFs) to help improve data quality in electronic data capture systems.
Q&A: How Sites and Sponsors are Collaborating to Move eSource Forward
Shannon Roznoski from Advarra and Michael Buckley from Memorial Sloan Kettering Cancer Center answer questions from a recent webinar.
How Sites and Sponsors are Collaborating to Move eSource Forward
April 6, 2020
In this webinar, Shannon Roznoski, Director of Product Management at Advarra-Forte and Michael Buckley, Manager, CRIT Enterprise Innovation at Memorial Sloan Kettering Cancer Center will discuss their experience as members ...
Reflections on SCDM 2019: Technology’s Role in Transforming Clinical Data Management
Advarra attended the SCDM Annual Conference earlier this month, and took the time to reflect on the growth of the clinical data management domain.
Data Collection in Clinical Trials: 4 Steps for Creating an SOP
Learn the necessary steps to create an effective SOP for data collection in clinical trials when using an electronic data capture (EDC) system.
5 Steps to Follow when Shopping for a Validated EDC System
Shopping for a validated EDC system can seem like a daunting task. Learn five steps that make the process less confusing.
How Paper and Electronic Source Data Meet ALCOA Elements
ALCOA ensures source data is safe and effective, but how does it differ for data collected on paper vs. electronically?