License/Certification/Education: Normally B.A./B.S. in Science w/1-2 years of experience.
Job Description:
Conducts audits for the regulatory/QA function within the Clinical Trials Department in order to help assure compliance with GLP/GCP in accordance with established FDA regulations and company policies and standard operating procedures.
Reviews data and reports emanating from laboratory Clinical Trials testing
Prepares timely reprots of the audit findings for distribution to management
Responsible for the tracking of the audit reports and teh comliance of all follow-up corrective action
Maintains current knowledge of GLP/GCP regulations and company policies and procedures
Maintains and provides Master schedule information and/or archive duties as assigned.
Job Description:
Conducts audits for the regulatory/QA function within the Clinical Trials Department in order to help assure compliance with GLP/GCP in accordance with established FDA regulations and company policies and standard operating procedures.
Reviews data and reports emanating from laboratory Clinical Trials testing
Prepares timely reprots of the audit findings for distribution to management
Responsible for the tracking of the audit reports and teh comliance of all follow-up corrective action
Maintains current knowledge of GLP/GCP regulations and company policies and procedures
Maintains and provides Master schedule information and/or archive duties as assigned.
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Job Title:
Quality Control Clinical Trials Auditor
Laboratory CorporationLocation:
Cranford, NJ
Status:
Full Time
Employee
Job Category:
Biotech/
R&D/Science
Requisition Number:
19477
Quality Control Clinical Trials Auditor
Laboratory CorporationLocation:
Cranford, NJ
Status:
Full Time
Employee
Job Category:
Biotech/
R&D/ScienceRequisition Number:
19477
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