Clinical study teams, and the IT groups that support their clinical operations, have access to a variety of eClinical systems (e.g. eTMF, CTMS, and other systems). Any one, or a combination of these, can be used to manage study startup documents and activities, as well as potentially drive process improvements and shorten overall timelines. However, without a clear understanding of the best uses of each eClinical system, it’s difficult to implement a solution that helps teams maximize collaboration, effectively manage document lifecycles, track metrics, and ensure compliance.
Join the webinar to discover future trends, assess available options, and implement an eClinical system that works best for your organization’s particular business requirements.
Featured speakers include Eldin Rammell, records management consultant and eTMF thought leader, and Dr. Rob Wynden, VP of Technology and Engineering for goBalto, an expert in biotech feasibility, subject identification, and study startup.
Eldin Rammell, Managing Director and Principal Consultant, Rammell Consulting
Eldin Rammell has over 25 years experience in the field of records management. His goal is to help organizations improve working practices, processes, and systems through the better use of information assets (records management can be a pivotal factor in achieving these improvements).
He is a frequent speaker at industry conferences including Records Management Society, MHRA Symposia, InfoTech Pharma, DIA, European Forum for Good Clinical Practice (EFGCP), CBI, ExL-Pharma, and Applied Clinical Trials. Eldin was a guest lecturer at City University, London and has published articles in the GCP Journal and Clinical Researcher.
He is an Executive Committee Member and past President of the Good Clinical Practice Records Managers Association (GCP-RMA) and Director in the Scientific Archivists Group.
Rob Wynden, VP of Technology and Engineering, goBalto
Rob Wynden has been a computer scientist and programmer for 28 years in the scientific programming, e-commerce, biotech, and health care industries. He implemented study startup and CTMS functionality at nine bay area biotech companies, and invented a method that allows medical and biotech organizations to use cloud-based analytics to monitor patient data.
He holds a BS in Computer Engineering from Sacramento State University and a PhD in Biological and Biomedical Clinical Informatics from UCSF.
Who Should Attend?
Clinical Operations management and IT professionals who work in clinical study startup
Premier Research is a leading global contract research organization serving biotech, Pharmaceutical and medical technology companies. The company has a wealth of experience in rare disease and pediatric research having managed about 100 projects in each area in the last five years alone. Its services include clinical research and regulatory outsourcing in the areas of analgesia; neurology; infectious, cardiovascular, and respiratory disease; dermatology; oncology; and medical devices.
Premier Research and operates in 50 countries. It employs 1,000+ clinical professionals dedicated first and foremost to fulfilling each customer’s requirements in a timely, accurate, and cost-effective manner. This includes a strong international network of monitors and project management professionals combined with regulatory, data management, statistical, scientific, and medical experts, and staff at its well-established network of dedicated clinical sites.