FEATURED JOBS
Start-up Specialist I
Regional,
Hong Kong
Job Overview
- Assist in preparation of project specific plans
- Collect, Review, Process and Track regulatory and investigator documents for effective and compliant study site activation
- Review and Customize Country and Site specific ICF (liaise with IRB/ICE on issues)
- Review and Update Documents with required revisions (site staff / amendments)
- Site contract and budget negotiation
- . .
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Start-up Specialist II
Indianapolis,
Indiana
Job Overview
We are seeking a Start-up Specialist for our Global Speciments Group in Raleigh, NC. Duties will include the following:
* Development and entry of Specimen Test Plans (STP)
* Assist in preparation of annual update of global Regulation and Guidance documents
* Assist Quality Assurance in regulatory certifications (ISO, Data Privacy, etc), validation processes, and SOP writing
Educat . .
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Clinical Quality Manager (Remote USA)
Orlando,
Florida
Job Overview
HQ CQM: CORE Accountabilities and Responsibilities
Overarching Responsibilities:
* Quality Management subject matter expert who provides real-time, proactive advice and guidance on procedures and issues relating to Quality, Compliance and Global Processes related to clinical development program management, clinical trial activities and vendor oversight.
* Ensures creation of the Qu . .
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Clinical Quality Manager (Remote USA)
Los Angeles,
California
Job Overview
HQ CQM: CORE Accountabilities and Responsibilities
Overarching Responsibilities:
* Quality Management subject matter expert who provides real-time, proactive advice and guidance on procedures and issues relating to Quality, Compliance and Global Processes related to clinical development program management, clinical trial activities and vendor oversight.
* Ensures creation of the Qu . .
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Clinical Quality Manager (Remote USA)
Dallas,
Texas
Job Overview
HQ CQM: CORE Accountabilities and Responsibilities
Overarching Responsibilities:
* Quality Management subject matter expert who provides real-time, proactive advice and guidance on procedures and issues relating to Quality, Compliance and Global Processes related to clinical development program management, clinical trial activities and vendor oversight.
* Ensures creation of the Qu . .
Read More