Site Management/Investigator Payments Featured Articles

  1. Are Sites Even Using AI?: How Sponsors And CROs Can Support Uptake 5/16/2025

    How much are clinical research sites using AI? And how can sponsors and CROs effectively support sites in doing so? Consultant Maria P. Ladd explains.

  2. 5 Ways AI Is Changing Clinical Research — And How To Embrace It 5/15/2025

    Discover how AI is transforming clinical trials, learn real tools already in use, and get practical guidance for clinical professionals — especially CRAs and site teams — looking to upskill in an AI-enhanced environment.

  3. 3 Strategies For A Successful Journey Toward Cell And Gene Therapy Commercialization 5/13/2025

    CTMC's Amy Hay provides 3 recommendations for teams developing cell and gene therapies, from clinical research through commercialization.

  4. The Potential Impact Of U.S. Tariffs On The Biotech Sector: Manufacturing, Funding, And Clinical Trials 5/12/2025

    Syner-G Biopharma Group's Raymond Forslund, Ph.D., MBA explores how U.S. tariffs might affect biotech manufacturing, funding, and clinical research.

  5. The Risk And Reward Of Clinical Investigators Integrating AI 5/1/2025

    Husch Blackwell LLP experts discuss relevant regulatory frameworks and the risks and liabilities of clinical investigators using AI.

  6. Run Better Trials By Rewriting The CRA-Site Relationship Playbook 4/29/2025

    Senior CRA Bryce Nichols explains how sites can use their CRAs — beyond their monitoring duties — to improve site efficiency, communication, and trial success.

  7. Japan's Adoption Of DCTs Is Slow But Steady 4/16/2025

    While global momentum for DCTs accelerates, Japanese healthcare institutions face unique structural and operational hurdles to implement remote and digital trial activities.

  8. From Tissue Donation To Distribution: Understanding EU Regulatory Requirements In Cell Therapy Clinical Trials 4/14/2025

    Understanding how the European Union's Directive 2004/23/EC interacts with GMP — and where its jurisdiction begins and ends — is essential for successful clinical trial planning, compliance, and execution.

  9. The Evolution Of A Clinical Research Coordinator 4/9/2025

    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). 

  10. Feasibility/Site Selection Process Ripe For Improvement 4/1/2025

    One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?