http://www.insourced.com/ RSS feed for Philadelphia, PA Field Investigator job search, from Insourced en-us admin@insourced.com admin@insourced.com RSS Feed Generator Aerotek Clinical Research is currently seeking an Associate Medical Director for one of our client sites in the Malvern, PA area for a temp to perm position. <br><br>DUTIES AND RESPONSIBILITIES<br><br>Responsible for successful implementation and operational aspects of Phase I to III clinical studies in the United States. <br>Direct/lead the Team to ensure successful completion of US Phase I, II and III clinical trials in a timely, ethical and a scientifically responsible fashion. <br>Evaluate ... http://www.insourced.com/job-listings/578785-associate-medical-director/ Fri, 19 Sep 2008 04:50:38 +5000 Aerotek Clinical Research is currently seeking an Associate Medical Director for one of our client sites in the Malvern, PA area for a temp to perm position. <br><br>DUTIES AND RESPONSIBILITIES<br><br>Responsible for successful implementation and operational aspects of Phase I to III clinical studies in the United States. <br>Direct/lead the Team to ensure successful completion of US Phase I, II and III clinical trials in a timely, ethical and a scientifically responsible fashion. <br>Evaluate ... http://www.insourced.com/job-listings/587625-associate-medical-director/ Fri, 26 Sep 2008 00:40:51 +5000 Aerotek Clinical Research is currently seeking an Associate Medical Director for one of our client sites in the Malvern, PA area for a temp to perm position. <br><br>DUTIES AND RESPONSIBILITIES<br><br>Responsible for successful implementation and operational aspects of Phase I to III clinical studies in the United States. <br>Direct/lead the Team to ensure successful completion of US Phase I, II and III clinical trials in a timely, ethical and a scientifically responsible fashion. <br>Evaluate ... http://www.insourced.com/job-listings/594616-associate-medical-director/ Fri, 03 Oct 2008 13:49:23 +5000 DUTIES:<br>-Identifies, evaluates and selects study centers <br>-Obtain, review for appropriateness and process regulatory and administrative documents from study sites<br>-Maintain clinical files<br>-Track progress and status of contractual agreements (non-disclosure agreements, clinical trial agreements, contracts with vendors)<br>-Manages central IRB, where applicable<br>-Process/track safety information (IND Safety Reports/SAE Reports) to ensure regulatory compliance and real-time reconcilia... http://www.insourced.com/job-listings/594607-senior-clinical-research-associate/ Fri, 03 Oct 2008 13:48:57 +5000