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Organization: WCG IRB. Job Type: Full Time - RegularThe IRB Affairs Specialist supports the IRB Review Board through administrative duties, supporting data collection, and the management and analysis of documents, client reporting, and problem resolution. This position will:Provide administrative support to the Board and clients by preparing...
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Organization: WCG IRB. Job Type: Part Time – TemporaryOur Document Processors are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time – TemporaryOur Document Processors are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time - RegularOur Document Specialist are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time - RegularOur Document Specialist are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time - RegularOur Document Specialist are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time - RegularOur Document Specialist are responsible for processing clinical study research documents and prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients. Over time you will...
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Organization: WCG IRB. Job Type: Full Time - RegularThe IRB QA & Compliance Associate is responsible for assisting and supporting the Compliance team with respect to establishing and maintaining quality assurance standards and measures across WCG services organization and ensuring such standards comply with regulatory requirements...
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Organization: WCG IRB. Job Type: Full Time - RegularThe IRB QA & Compliance Associate is responsible for assisting and supporting the Compliance team with respect to establishing and maintaining quality assurance standards and measures across WCG services organization and ensuring such standards comply with regulatory requirements...
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