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	<title>Comments for The Clinical Trials GuruThe Clinical Trials Guru</title>
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	<description>Discussing Clinical Trials In Plain English</description>
	<lastBuildDate>Fri, 24 May 2013 00:27:36 +0000</lastBuildDate>
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		<title>Comment on When And How To Invoice For Different Fees In Clinical Trials by Stacey Carmody</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/when-and-how-to-invoice-for-different-fees-in-clinical-trials/#comment-66629</link>
		<dc:creator>Stacey Carmody</dc:creator>
		<pubDate>Fri, 24 May 2013 00:27:36 +0000</pubDate>
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		<description><![CDATA[Very good. Don&#039;t forget the IRB fees too! You want to make sure those costs are covered!]]></description>
		<content:encoded><![CDATA[<p>Very good. Don&#8217;t forget the IRB fees too! You want to make sure those costs are covered!</p>
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		<title>Comment on How A Clinical Research Study Coordinator Can Keep Their Source Documentation Organized by Stacey Carmody</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/how-a-clinical-research-study-coordinator-can-keep-their-source-documentation-organized/#comment-66628</link>
		<dc:creator>Stacey Carmody</dc:creator>
		<pubDate>Thu, 23 May 2013 23:47:07 +0000</pubDate>
		<guid isPermaLink="false">http://theclinicaltrialsguru.com/blog1/?p=5279#comment-66628</guid>
		<description><![CDATA[I work in a large hospital setting we have our own internal drives and networks and programs so we don&#039;t need to use an outside application like Google, etc. I couldn&#039;t tell you about those types since I never used them.]]></description>
		<content:encoded><![CDATA[<p>I work in a large hospital setting we have our own internal drives and networks and programs so we don&#8217;t need to use an outside application like Google, etc. I couldn&#8217;t tell you about those types since I never used them.</p>
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		<title>Comment on Can A Doctor With Little Research Experience Ever Become A Principal Investigator Of A Clinical Trial? by Dan Sfera</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/can-a-doctor-with-little-research-experience-ever-become-a-principal-investigator-of-a-clinical-trial/#comment-66619</link>
		<dc:creator>Dan Sfera</dc:creator>
		<pubDate>Thu, 23 May 2013 04:21:19 +0000</pubDate>
		<guid isPermaLink="false">http://theclinicaltrialsguru.com/blog1/?p=5282#comment-66619</guid>
		<description><![CDATA[Stacey, as always you are spot on, and are giving me more ideas for future posts.  I think I will do one entitled &quot;Its all about the CV&quot;]]></description>
		<content:encoded><![CDATA[<p>Stacey, as always you are spot on, and are giving me more ideas for future posts.  I think I will do one entitled &#8220;Its all about the CV&#8221;</p>
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		<title>Comment on Can A Doctor With Little Research Experience Ever Become A Principal Investigator Of A Clinical Trial? by Stacey Carmody</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/can-a-doctor-with-little-research-experience-ever-become-a-principal-investigator-of-a-clinical-trial/#comment-66618</link>
		<dc:creator>Stacey Carmody</dc:creator>
		<pubDate>Thu, 23 May 2013 02:31:24 +0000</pubDate>
		<guid isPermaLink="false">http://theclinicaltrialsguru.com/blog1/?p=5282#comment-66618</guid>
		<description><![CDATA[The answer is YES, I do agree. Most doctors  have had some research experience of some sort while residents, and especially as fellows. Fellowships in a specialty last anywhere from a year to 4 years and usually include research of some kind or another. I agree sub I&#039;s stand a  good chance of becoming a PI if they have been sub I&#039;s on a handful of trials. It&#039;s all about the CV. This is what Sponsors look at - the CV and the research experience on it.]]></description>
		<content:encoded><![CDATA[<p>The answer is YES, I do agree. Most doctors  have had some research experience of some sort while residents, and especially as fellows. Fellowships in a specialty last anywhere from a year to 4 years and usually include research of some kind or another. I agree sub I&#8217;s stand a  good chance of becoming a PI if they have been sub I&#8217;s on a handful of trials. It&#8217;s all about the CV. This is what Sponsors look at &#8211; the CV and the research experience on it.</p>
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		<title>Comment on How A Clinical Research Study Coordinator Can Keep Their Source Documentation Organized by Dan Sfera</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/how-a-clinical-research-study-coordinator-can-keep-their-source-documentation-organized/#comment-66617</link>
		<dc:creator>Dan Sfera</dc:creator>
		<pubDate>Thu, 23 May 2013 00:45:28 +0000</pubDate>
		<guid isPermaLink="false">http://theclinicaltrialsguru.com/blog1/?p=5279#comment-66617</guid>
		<description><![CDATA[yes, subfolders are good.  What shared drive do you guys use? does google drive allow for &quot;subfolders&quot;]]></description>
		<content:encoded><![CDATA[<p>yes, subfolders are good.  What shared drive do you guys use? does google drive allow for &#8220;subfolders&#8221;</p>
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		<title>Comment on How A Clinical Research Study Coordinator Can Keep Their Source Documentation Organized by Stacey Carmody</title>
		<link>http://theclinicaltrialsguru.com/blog1/2013/05/how-a-clinical-research-study-coordinator-can-keep-their-source-documentation-organized/#comment-66614</link>
		<dc:creator>Stacey Carmody</dc:creator>
		<pubDate>Thu, 23 May 2013 00:16:45 +0000</pubDate>
		<guid isPermaLink="false">http://theclinicaltrialsguru.com/blog1/?p=5279#comment-66614</guid>
		<description><![CDATA[Agree that a shared drive is great. My site uses a shared drive. You just have to make sure all the folders on it are clearly named with the protocol name. Then have &quot;sub-folders&quot; called &quot;Consents&quot;,  &quot;Full Protocol&quot;,&quot;IRB&quot;, &quot;Sponsor Letters&quot;, &quot;List of Subjects&quot;, etc.]]></description>
		<content:encoded><![CDATA[<p>Agree that a shared drive is great. My site uses a shared drive. You just have to make sure all the folders on it are clearly named with the protocol name. Then have &#8220;sub-folders&#8221; called &#8220;Consents&#8221;,  &#8220;Full Protocol&#8221;,&#8221;IRB&#8221;, &#8220;Sponsor Letters&#8221;, &#8220;List of Subjects&#8221;, etc.</p>
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