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The Benefits of Working for a Rapidly Growing Global Clinical Research Organization (CRO) like Medpace

XTalks

A clinical research organization (CRO) is a company that delivers outsourced services to plan, manage and execute clinical trials for biotechnology, pharmaceutical, and medical device companies. Read on to learn why life science and clinical research professionals are choosing a career with Medpace.

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“Nothing scares us” – Ukraine’s clinical research sector begins fearless recovery

Drug Discovery World

Following the news that the number of clinical trial recruiting sites in Ukraine has dropped by half since the Russian invasion, DDW’s Diana Spencer examines clinical trial data from analytics company Phesi and speaks to Dr Olena Karpenko , Clinical Research Director at Medical Center Ok!Clinic+ Dr Olena Karpenko.

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NORD’s Dr. Neilan Discusses Next Steps for Rare Disease Clinical Trials

XTalks

NORD, along with its more than 330 member patient organizations, is committed to the identification, treatment and cure of rare disorders through education, advocacy, research and patient services. Since only about 5 percent of rare diseases have FDA-approved treatments, it is vital that we increase the pace of rare disease clinical research.

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Wearable Biosensors for Decentralized and Hybrid Clinical Trials

XTalks

The way in which clinical trials are conducted is entering a new dimension as clinical trial operations are becoming more adaptable. Richard Lee, MD, Senior Medical Director of the Medical Department at the global contract research organization (CRO) Medpace. What are Decentralized and Hybrid Clinical Trials?

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Considerations for Neuroscience Trials with Intrathecal Delivery and Other Methods of Direct CNS Administration

XTalks

Clinical research experts from the CRO Medpace shared insights about the operational and regulatory considerations for neuroscience trials with direct CNS administration. In a recent webinar, Dr. Vornov described the history and current progress in targeted CNS therapeutic delivery.

Trials 83
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Cardiac Biomarkers in Cardiovascular Clinical Trials: Caveats and Considerations

XTalks

Even if a robust cardiac biomarker is identified, it can run into regulatory hurdles, which is why close relationships between sponsors and regulators is critically important in order to reduce time to qualification, making it important to work hand in hand, Dr. Januzzi says. A Functional Future State.

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Avoiding Radiation Toxicity: Understanding Dosimetric Endpoints and Challenges in Radiopharmaceutical Clinical Trials

XTalks

A clinical research coordinator (CRC), data coordinator or study nurse may be the first to note a potential MR note or exam finding that must be escalated to the investigator for immediate review.