This is a full-time position in Dallas TX to supervise co-ordinate and lead clinical trial specific activities in accordance with Sponsor and CRO SOP s ICH-GCP requirements and local regulations. This individual will report to the Clinical Operations Manager and serve as the primary contact with the sponsor and research sites. The ideal candidate will have GCP expertise and at least 3 years in a project managerial role with a CRO Pharmaceutical company. Duties and responsibilities of the Project Manager Include Reviewing monitoring reports as part of Quality Control program Developing reviewing and editing of project plans to assure consistency with project...read moreApply NowCompany
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Manufacturing Engineer (CNC Design) - Canton OH - JOB 24-00765Salary Range 60K - 85K Permanent...
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