“SCDM is the organization that brings pharma, CROs, technology companies and regulators together from across the globe, accelerating innovation to drive science to improve the health of humanity.”
SCDM – through its remarkable international Annual Conference – has been championing clinical data management (CDM) excellence since 1994 with the goal of providing the benchmark for CDM knowledge and education that drives progress in the industry
Plan your conference and trip to #SCDM2022.
Your essential guide to the conference with real-time updates.
We run the SCDM Annual Conference for anyone in the clinical data management industry who believes in applying thought leadership and practical content to advance the role of CDMs. The SCDM Annual Conference exists to drive progress across the world and to support the evolution from Clinical Data Management toward Clinical Data Science.
At SCDM 2022, you can expect a meeting of minds, practical insights, workshops, big idea presentations and, of course, exciting debate formats to encourage the sharing of the latest insights and learnings for greatest impact, between industry experts from all over the world.
Regular rates deadline
Director, Program Lead, Data Monitoring and Management, Pfizer
Carol, an Asset Lead in the Inflammation and Immunology therapeutic area at Pfizer, has 25+ years of Pharma experience where she started in research as a protein biochemist and moved into the Clinical Data Management arena in 2000. She has experience in both Early and Late Phase clinical development, both in project management as well as line management.
Her therapeutic areas of experience are in Cardiovascular, Metabolism, Inflammation, Immunology, Infectious Diseases, Rare Diseases and Ophthalmology and she also has expertise in all aspects of outsourcing, including study and project oversight as well as global team leadership and governance. Carol holds both Bachelor’s and Master’s degrees in Biology (specializing in Biotechnology) from William Paterson University.
Managing Director Accenture Solutions Pvt Ltd
Shobhit Shrotriya is an experienced professional in Accenture’s Life Sciences R&D practice based out of Bangalore. He is an Engineer by training with a Masters in Industrial Management from Indian Institute of Technology (IIT) Kanpur. He is a Certified Six Sigma Black Belt and Project Management Professional (PMP).
With 20+ years of work-experience Shobhit has extensive experience in Operations Management, Project & Program Management, Process Excellence and Innovation. Shobhit is a Subject Matter Expert who contributes to the solution development, process re-engineering, and implementation of life sciences outsourcing service delivery. With extensive experience in life sciences operations, he has managed end to end global projects and large customer accounts with an excellent track record of delivering mega-scale projects on time, under budget and with high standards of quality.
Shobhit has been associated with leading industry forums such as Project Management Institute, DIA and SCDM over the years where he has contributed both as a presenter and a session chair.
In his current role as Accenture Global Lead for Life Sciences R&D Operations, Shobhit is responsible for providing comprehensive domain expertise and driving standardization of processes and best practices across client teams.
Associate Director, Clinical Data Management, ICON
Twenty-four years of biotechnology, microbiology and clinical trial data management. Areas of focus include recombinant, subunit, attenuated and whole-cell bacterin, and viral vaccines, oncology, gout, and biosimilar studies as well as monoclonal therapies. Significant exposure to global team leadership, project management, and data operations functional management support for local and global team members, including clinical data coordinators, lead data managers and functional managers. SCDM panel chair in 2018, 2019 and 2021. SCDM conference Co-Chair 2020, 2021.
Vice President, Vault CDMS Strategy Veeva Systems
A veteran of almost 25-years in life sciences, Richard is Vice President, Strategy, Vault CDMS. Richard is responsible for defining strategy and direction for Vault CDMS, especially with respect to clinical data management. Richard brings Veeva customers both keen executive vision and proven operational experience in data management, eClinical Solutions, and advanced clinical strategies (e.g. adaptive trials, risk based monitoring, strategic technology reviews).
Richard has overseen the transition from concept to delivery of initially EDC, and now CDMS, and assists customers and partners in their strategic future setting.
Richard’s extensive background in clinical data management, operational excellence, strategic planning, marketing, and business development enable him to provide fresh insights to clinical strategies.
Reconnect with the global Clinical Data Management community, celebrate imaginative ideas and pioneering mindsets, and get inspired at SCDM 2022.