Site Management

Latest Site Management Resources

7 Staff Augmentation Resources to Help Your Site Restart Research

With research activities gradually resuming, research teams may be challenged with conducting their trials effectively and efficiently. Here’s how Staff Augmentation can help.

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Improving Site-Sponsor Relationships Leads to Transparent Clinical Trials

The site-sponsor relationship is a multi-faceted one. The need for communication and understanding between the two is prevalent now more than ever.

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Patient Engagement and the IRB

The research community has increased patient and participant engagement, potentially impacting IRB review

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For Sponsors and Sites, the Research Restart Effort Begins with Communication

The global pandemic has changed the way we think about research. Sponsors should consider how the “new normal” will impact sites and current studies as they plan to re-start research.

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Finding a “New Normal” in Clinical Research

For much of 2020, COVID-19 has challenged “normal,” daily lives of many, but what does that mean for clinical research?

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4 Essential Skills for the Ideal Clinical Trial Project Manager

Learn how to find the right individual to manage your clinical research projects and improve the efficiency of your clinical trials.

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Trial Design in the Time of COVID-19: Complex and Efficient

While the clinical research community is currently being challenged by the COVID-19 pandemic, adaptive and platform study designs may provide much-needed help for sites.

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Generating Leadership Buy-In for a Clinical Research Business Intelligence Solution

Strategies for convincing leadership to invest in the tools needed to optimize operations and inform strategic decision-making.

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Keep in Touch: Tips for Working with a Single IRB for the First Time

Recent regulations and policies have ushered in the era of mandated single IRB (sIRB) review. Many institutions must now establish policies and processes for working with an external sIRB.

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Beginner’s Guide to Investigational New Drug and Investigational Device Exemption

When conducting an investigator-initiated trial, oftentimes, an investigational new drug or investigational device exemption application is necessary. Learn more about IND and IDE reporting.

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