Clinical Quality Specialist

GlobalChannelManagementInc

La Jolla Ranch, CA, United States contract

Posted: August 24, 2017

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Quick Summary

Clinical Quality Specialist is responsible for ensuring the quality of clinical trials by conducting quality control and assurance activities, and providing training and support to clinical trial staff.

Required Skills

Medical Technology Quality Management System Molecular Biology Laboratory Standard Operating Procedures

Job Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Clinical Quality Specialist needs BS/MS in a biological science, pharmacy, medical technology, or a related field

Clinical Quality Specialist requires:

• Medical Technology, MT (ASCP) license or equivalent (preferred)
• At least 2 years’ experience working in a laboratory setting that included a QMS
• Good working knowledge of GCP/GCLP guidelines
• molecular biology and laboratory safety procedures for handling hazardous chemicals and biosafety level 2 biohazard materials

Clinical Quality Specialist duties:

• Maintain, troubleshoot, and monitor the effectiveness of the POCRL’s Quality Management System (QMS)
• Ensure that POCRL activities conform with the requirements of the laboratory QMS
• Coordinate
creation, approval, implementation, and periodic reviews of novel
Standard Operating Procedures for the POCRL according to GCLP guidelines

$36/hr

12 months

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