Clinical Data Strategy in Action for Complex Clinical Trials
Webinars
April 25, 2024
Automating the Clinical Data Pipeline for Enhanced Data Review & Analytics
There has been a dramatic increase in clinical data types, sources and systems in recent years enabling new insights into patient experiences while also presenting challenges in consolidating, standardizing and analyzing these new data streams. The tools for centralizing, integrating, mapping and analyzing data have not kept pace with research and are causing cycle time delays and require numerous manual processes. This webinar will describe how new platforms like the elluminate Clinical Data Platform are automating the ingestion of data from numerous eClinical systems and sources, enabling faster data mapping and standardization, supporting risk-based data review and advancing both clinical and operational analytics. Key value drivers for these platforms including results from the Tufts Center for the Study for Drug Development (CSDD) and eClinical Solutions Data Strategies and Transformation Study will be discussed.
Who Should Attend
This webinar will appeal to individuals with the following or related job titles working at CROs, pharma or biotech companies:
- Vice President/Director/Sr. Director Clinical Operations
- Directors/Managers Clinical Programming
- Vice President/Director/Sr. Director Clinical Development Operations
- Director/Sr. Director/Clinical IT
- Sr. Director/Director/Associate Director Clinical Data Systems
- VP/Sr. Director/Director/Assoc. Director Clinical Data Management
- Sr. Director/Director/Assoc. Director Biostatistics/Bioinformatics
What You Will Learn
- What a clinical data pipeline is and how it works
- Key industry challenges a clinical data pipeline and centralized platform addresses
- Enhanced methods of clinical data review using data workbenches and analytics
- Value and return an automated data pipeline and clinical data platform delivers
Presenters
Vice President, Business Development Operations, eClinical Solutions
Dawn has over 20 years of experience in the pharmaceutical industry. She has worked within every level of clinical data management, from Data Coordinator to Senior Director where she participated in or had oversight for more than 250 clinical trials. During her time in the industry, she has provided consultation to organizations on clinical trial conduct, best practices in Data Management and data capture as well as developed standardized libraries and templates to support the adoption of CDISC standards. She is an active member of SCDM as a GCDMP SME, course designer and webinar presenter as well as Co-Chair of the annual conference (2018-2021) and serves on the SCDM Board of Trustees. Dawn is involved as a member of the CDISC-CDASH core team, Diabetes sub-team, CDASH CFAST Expanded Leadership Team and former Co-Chair of the CRF Library project. Dawn currently holds the position of Vice President, BD Operations, where she supports business development as a Clinical Subject Matter Expert for both software and data services as well as overseeing the Proposals and Solution Consulting departments.
Former Chief Marketing Officer, eClinical Solutions
Sheila has more than 20 years of industry experience including marketing, product management and strategy roles in life sciences technology companies. She spent 15 years at PHT Corporation (now ERT) in a variety of marketing and executive leadership roles helping to drive the company’s growth and the industry adoption of electronic clinical outcome assessments (eCOA). At eClinical Solutions, Sheila managed all aspects of marketing including branding, communications, lead generation and product marketing. She enjoys finding creative ways to tell customer stories, and building products and services that help clinicians, data scientists and technologists do the challenging and important work of bringing life-saving new therapies to market.
