Newsletter | April 18, 2025

04.18.25 -- How AI Models Can Actually Improve eTMF Management

TRIAL MONITORING

The Evolution Of A Clinical Research Coordinator

Briana White is a CRC with Superior Clinical Research, a small clinical research site in Smithfield NC. She talks about how she got into the clinical industry and what she struggles with in her job (spoiler alert: it involves tech). 

The Critical Role Of The Medical Monitor

Medical Monitors interact with nearly all functional roles on a study team and more experienced monitors often support and mentor less-experienced colleagues.

CLINICAL DATA MANAGEMENT & ANALYTICS

How AI Models Can Actually Improve eTMF Management

GCP consultant Donatella Ballerini explores how AI is shaping eTMF management and what this means for the future of clinical research in part one of this series.

Data Analytics: Driving Commercialization And Clinical Success

Advanced analytics enable life sciences companies to optimize the trials, facilitating data-driven decisions that significantly reduce the time and financial burdens associated with drug development.

From Data Silos To Unified Insights: The Power Of AI In Clinical Trials

AI tools like TrialKit AI revolutionize clinical trials by integrating diverse data sources, including wearables, breaking silos, enhancing insights, and enabling smarter, more patient-centered research.

Data-Driven Adaptive Trials Enhance Safety, Progress, And Economics

By offering guidance on optimizing ROI from extensive data collections and various endpoints in clinical studies, learn how IRT technology can enhance the data-driven approach for sponsors.

Maximizing Clinical Data Insights With Advanced Analytics Platforms

To achieve drug approval, trials must collect, combine, and analyze diverse data sets that support operational, safety review, risk management, and other analyses crucial to development.

The Importance Of Category Expertise In Cardiovascular Research

Developing life-saving heart health treatments requires an understanding of the unique requirements of cardiovascular studies, along with flexible eClinical and electronic data capture solutions.

Regulated Document Review

Enables secure real-time document review, co-authoring, and redaction in order to shorten the document review process by up to 65%.

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  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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