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DSI had this come up at a Sponsor induced audit for a pain mgt. Drug Study trial where they asked me if it were not a violation of GCP to have subjects fast for V1 prior to their signing the ICF. My response was consent is a process; the most proximal is the ad, then the V1, etc.... I explained our process of how to minimize harm and maximize benefit. I enquired if she had knowledge of how to do it better, and she did not. I called the Sponsor to enquire about her and they told me to ignore thi8s silly question.
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I don't think this should be a practice that we allow. What if something happened to the monitor or if the docements got stolen? There would be information floating around out there. After all coordinators are not to take source documents off site.
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BioPharma Research, located in Coral Gables, Florida is seeking PI's and sub-PI's for this multi-specialty group practice. Great opportunity in sunny South Florida. Three to five year clinical trial experience and a valid Florida Medical license are a must.
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Free compliance management systems for investigative sites, sponsors and CROs.
http://www.trainingcampus.com/petsite.aspx
You are cordially invited to attend my presentation in the Exhibit Hall during the ACRP conference in Houston, Texas at the
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Our site, Finger Lakes Clinical Research has an immediate opening for a Clinical Study Coordinator with two or three years experience in clinical trials. We are a small but rapidly growing, independent and very busy site involved mostly in CNS trials (depression, bipolar, schizophrenia, cognition). Great working conditions in the heart of Brighton at 12 Corners.
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Longmont Medical Research Network, located in Longmont, Colorado in the foothills of the Rocky Mountains, is seeking a Clinical Director of Research for this multi-specialty, group private-practice. We have been conducting pharmaceutical clinical trials for over 25 years and enjoy a great reputation with pharma and CROs alike. This is a great opportunity for the right person - looking for someone with a clinical background and at least 5 years of clinical trial experience. BSN preferred. see our website at
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