Clinical Research Associate (CRA)- 3-5 Years experience (North Chicago)

  • Address:North Chicago, IL 60064 (map)
  • Date Posted:08/26/16
  • Job Type:Full-time
  • Description:
  • The manager provided the following information: I need candidates that have written protocols, done global submissions, managed CROs, wrote ICFs, and other general study management activities. She said the candidates she has seen so far do not have this experience Manager is looking for study management experience!! Clinical Research Associate (CRA)-North suburbs of Chicago11528 40-50.00 an hour w2 contractStart date asap. 09/26/2016 to 08/25/2017Primary responsibilities will be to conduct remote monitoring activities in house for one or more studies. Experience with EDC is required. Safety review experience preferred.Other potential responsibilities may be to assist Study Project Manager (SPM) for one or more clinical studies.• Assist with management of vendors such as Clinical Research Organizations (CRO), Central Lab and other suppliers.• Work with other functional areas.• Responsible for compliance with applicable Corporate and Divisional Policies and procedures.• Assist SPM in planning and management of one or more clinical studies.• Assist SPM in the coordination of activities of cross-functional areas for the initiation, conduct and completion of one or more clinical studies on time and within budget (track expenditures).• Coordinate study activities such as study design, protocol preparation, investigator selection, investigator meeting and contract preparation, vendor selection & CRF design and other activities to ensure on time completion of studies.• Assist SPM in assessment of study conduct, development of monitoring plan and progress of study for adherence to the plan.• Identify site issues that potentially impact evaluable study data, ethical study conduct and ICH compliance.• Identify and escalate issues impacting study hygiene and make recommendations for corrective action.• Liaison with functional areas contributing to the outcome of clinical studies.• Assist in the management of study completion activities through timely oversight of CRF collection, DCF resolution, site-close out activities and activities of other contributing/cross functional areas.• Coordinate activities of study vendors that are necessary for completion of study and availability of data for analysis.• Assist in planning and execution of meetings and may present at Investigator Meetings and may assist Medical Writing in data line listings, statistics table review, or QCl3-5 yrs of exp.
Ad ID: 45764272
  • Posted by: Ad Partner | View all ads
  • Profile: Active since 08/2016
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