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
Spherion is hiring Customer Service Representatives immediately in Asheville, NC. The ideal candidate will have at least one year of experience in a customer service position. These positions are fast-paced and require high levels of computer and phone use, often using multiple computer screens.Working Hours: 8:00AM - 5:00PM, Monday - FridayResponsibilities:-Take incoming calls and provide answers to frequently asked questions-Assist customers in a timely
Spherion is hiring Customer Service Representatives immediately in Asheville, NC. The ideal candidate will have at least one year of experience in a customer service position. These positions are fast-paced and require high levels of computer and phone use, often using multiple computer screens.Working Hours: 8:00AM - 5:00PM, Monday - FridayResponsibilities:-Take incoming calls and provide answers to frequently asked questions-Assist customers in a timely
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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