UCB’s Post

Wondering what it is like to work in the Veramed Clinical Data Management team? Check out this month's #VeraPeople interview with Nathan Efferson, Senior Clinical Data Manager. Please reach out if you are interested in learning more about Veramed's Clinical Data Management team! #WeAreVeramed #DataManagement

Faces Of Premier: A Look At The People Of Clinical Trials Rostislav Marinov Associate Data Coordinator at Premier Research uses knowledge of EDC systems and study data requirements when performing his role, which is beneficial to the clinical trial and the organization. I thank, value and appreciate Rostislav for passion for clinical research and bringing that passion to Premier. #Art #ClinicalTrials #OneTeam #PremierPeople #PremierResearch

It’s truly a transformative era for Clinical Research Associates (CRAs). As Helen Yeardley, Senior Vice President, Global Clinical Operations at ICON plc, brilliantly outlines in her article, “The CRA of the Future: From ‘Road Warrior’ to Site ‘Owner’”, the CRA role is pivotal to the success of clinical trials and is evolving rapidly in response to the industry’s dynamic changes. At Clinova, we’re keenly aware of these shifts in CRA demand and the expansion of their responsibilities. The transition from being predominantly on the road to taking on a more holistic ‘site owner’ role signifies a significant development in how we approach clinical trials. It’s about adapting with agility and supporting our CRAs with the necessary skills and training for these new challenges. We commend ICON plc for leading the conversation on this topic and look forward to integrating these insights into our own practices. This article is a must-read for anyone in the field looking to understand and navigate the future landscape of clinical research talent. #ClinicalResearch #CRA #FutureTrends #Clinova #ICON

As no two projects are identical, nor all risks considered equal, IQVIA tailors its validation strategy to the volume, complexity and risk level of each deliverable. This thoughtful and precise approach to quality control allows our teams to selectively redistribute resources to enhance scrutiny of higher-risk data— optimizing overall code quality, improving accuracy, and speeding up response times. Learn more with IQVIA’s Risk-Based Validation fact sheet. https://bit.ly/3YecJSM #FSP #datavalidation #riskbasedvalidation

The responsibilities of a clinical data manager are becoming increasingly complex and demanding... As clinical research and clinical data management continue to evolve and innovate, the demands on professionals in this field increase. The role of a clinical data manager has become more complex, requiring a constantly changing skill set to keep pace with cutting-edge technology. One of the key challenges is staying abreast of these changes while also understanding developments in other organisations. This is where the Association for Clinical Data Management (ACDM) plays a crucial role, offering support and resources to help the sector to navigate this dynamic landscape. For over 35 years, the ACDM has been at the forefront of the global clinical data management community, supporting it through a period of continuous change. The ACDM facilitates this support through various initiatives, including Data Management Expert Groups, Hot Topics discussions, Symposium Events, and the Annual Conference. These activities provide valuable opportunities for professionals to stay updated on industry trends, share knowledge, and enhance their skills, ensuring they are well-equipped to meet the ever-evolving demands of the sector. Find out more about the ACDM here: https://acdmglobal.org/ Robert King, Sverre Bengtsson, Jo Marshall, Nina Reyes, Eva Alder, Amelie Spieser, Anita Kratchmarov, Nicola Götz, Ashley Howard, Richard Davies #clinicaltrials #clinicalresearch #clinicaldatamanagement #acdm

As no two projects are identical, nor all risks considered equal, IQVIA tailors its validation strategy to the volume, complexity and risk level of each deliverable. This thoughtful and precise approach to quality control allows our teams to selectively redistribute resources to enhance scrutiny of higher-risk data— optimizing overall code quality, improving accuracy, and speeding up response times. Learn more with IQVIA’s Risk-Based Validation fact sheet. https://bit.ly/3YsdbhV #FSP #datavalidation #riskbasedvalidation

And it gets even more interesting when we integrate with other systems in the ecosystem like patient recruitment,EHR, live feasability analyses and more. The image below shows one more thing. Right brain is the creative side. The new side of the Data Manager.

🚀 Day 21- Mastering Clinical Data Management 🚀 In the Conduct Phase, Listings play a crucial role in ensuring data quality, accuracy, and compliance with the study protocol. 💡 What are Listings? Listings are tabular representations of trial data that allow for detailed review, validation, and reconciliation of clinical data. ✨ Key Uses of Listings in CDM: 1. Data Review & Quality Control: Regularly reviewing subject, site, and visit listings ensures that data is accurate and complete. 2. Query Management: Identifying data discrepancies through listings helps us raise and resolve queries efficiently. 3. SAE Reconciliation: Listings aid in reconciling serious adverse events (SAEs) across clinical and safety databases, ensuring consistency. 4. External Data Reconciliation: By comparing lab results and third-party data with clinical data, listings help catch discrepancies early on. 💼 As Clinical Data Managers, we generate and review these listings regularly to ensure data integrity throughout the study. #ClinicalDataManagement #ClinicalTrials #DataIntegrity #Listings #CDM #ClinicalResearch #DataQuality #LifeSciences #Day21 #Data #datamanagement #Clinical #datamanagement #DATA #Datalistings #Listings

Clinical data management involves the collection, validation, and storage of data generated during clinical trials in accordance with regulatory standards and protocols. It ensures the accuracy, completeness, and integrity of clinical trial data to support decision-making and regulatory submissions. Follow us on Social Media: https://lnkd.in/gHAyMjQ2 🌐 Website: truelessons.io 📧Email: [email protected] 📞 Call: +91 9620000023 #ClinicalDataManagement #DataAccuracy #RegulatoryCompliance #ClinicalTrials #DataIntegrity #DataValidation #ResearchStandards #ClinicalResearch #DataCollection #DecisionSupport #ProtocolAdherence