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    <title><![CDATA[investigator - Trovit]]></title>
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        <url>http://jobs.trovit.co.uk/images/global/logopowered2.png</url>
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    <link>http://jobs.trovit.co.uk/</link>
    <description><![CDATA[New ads in Trovit]]>
	
	</description>
    <language>en_UK</language>
        <item>
        <title><![CDATA[Senior Computer Forensics Investigator]]></title>
        <description><![CDATA[ London <br />Senior Computer Forensics <strong>Investigator</strong> location: London (City) salary:<br /><strong>£47500 </strong><strong>Permanent</strong> <br />20/08/2008 in Jobsite]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7694261/what.investigator/pos.1/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Associate Medical Director - Cambridge]]></title>
        <description><![CDATA[ Cambridge <br />Associate Medical Director - Cambridge Key areas of responsibility include providing project-specific clinical research medical services and medical support for pharmacovigilance and medical information services. You will help plan, prepare and review/approve regulatory submissions, protocols, <strong>Investigator</strong> Brochures, among other documents. In addition you will provide a specialist<br /><strong>£50000 </strong><br />20/08/2008 in Experteer.co.uk]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7687118/what.investigator/pos.2/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Scientific and Technical - Clinical Research]]></title>
        <description><![CDATA[ Berkshire <br /><strong>Investigator</strong> Brochures • To create and write the International Technical Protocols and design the primary and secondary... country and <strong>investigator</strong> feasibility assessment for the CROs. • To train all partners (Clinical Project Manager, CRAs etc) on.... • To prepare the medical section of the monitoring guide and medical review guide. • Participate at <strong>inves<br /><strong>£67500 </strong><strong>Any</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4medical]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7685682/what.investigator/pos.3/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Scientific and Technical - Clinical Research Associate]]></title>
        <description><![CDATA[ Berkshire <br />, <strong>investigator</strong> brochures, and supporting regulatory documentation. • Ability to provide strategic regulatory advice to clients on their proposed clinical development plan. • Able to assess CMC, preclinical and clinical data for NCEs, biotechnology and other...<br /><strong>£45000 </strong><strong>Any</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4medical]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7685702/what.investigator/pos.4/referer_id.3</link>
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        <item>
        <title><![CDATA[Scientific and Technical - Project Manager]]></title>
        <description><![CDATA[ Berkshire <br /><strong>investigator</strong> meetings. - Completes trial commitment forms assuring best outcome according to ICRO metrics and approves budget allocation. - Negotiates contracts with CROs, SMOs and NHS trusts. - Develops recruitment strategies and contingencies in...<br /><strong>£32000 </strong><strong>Any</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4medical]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7685707/what.investigator/pos.5/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Clinical Research - CRA, Clinical Study Coordinator]]></title>
        <description><![CDATA[ Any Location <br />of audits activities (report, review and tracking of corrective actions, self-inspections) -Conduct audits (3rd party, <strong>investigator</strong> sites, internal systems) -Review SOP and WP to ensure compliance with regulatory requirements -Support GxP training and...<br /><strong>£66000 </strong><strong>5 years</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4dd]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7684916/what.investigator/pos.6/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Regulatory And Drug Safety - Clinical Project Manager, Drug Safety, Pharmacovigilance]]></title>
        <description><![CDATA[ Cambridgeshire <br />documents, ICSR submission, <strong>investigator</strong> letter, and CCSI distribution. Understanding the data requirements of E2B submission. Working with Clinical Research and CROs, regarding information exchange and safety exchange agreements. Recognising...<br />Negotiable</strong> <strong>N/A</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4dd]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7684927/what.investigator/pos.7/referer_id.3</link>
    </item>
        <item>
        <title><![CDATA[Physicians - Toxicology, Medical Advisor]]></title>
        <description><![CDATA[ Cambridgeshire <br />key opinion leader advisory groups for each product/therapeutic area. Supporting the development of clinical data through clinical trials and <strong>investigator</strong> studies. Analysing trial data and providing interpretation to marketing and sales...<br />Negotiable</strong> <strong>N/A</strong> <strong>Permanent</strong> <br />20/08/2008 in jobs4dd]]></description>
        <link>http://jobs.trovit.co.uk/scripts/redirect.php/id.7684938/what.investigator/pos.8/referer_id.3</link>
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