We are looking for detail-oriented Temporary Administrative Assistant for a Manufacturing site in Arden,NC to support a special short-term project focused on improving document management within our Quality Management System. In this role, you will assist in organizing, reviewing, and standardizing documentation to ensure full compliance with internal procedures and industry standards such as IATF 16949. This is a temporary, 3-month contract assignment off
We are looking for detail-oriented Temporary Administrative Assistant for a Manufacturing site in Arden,NC to support a special short-term project focused on improving document management within our Quality Management System. In this role, you will assist in organizing, reviewing, and standardizing documentation to ensure full compliance with internal procedures and industry standards such as IATF 16949. This is a temporary, 3-month contract assignment off
The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
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