We are looking for an EHS Manager to lead our safety and environmental programs at our manufacturing facility in Salt Lake City, Utah. In this role, you will lead a team to make sure our workplace stays safe, healthy, and up to date with all state and government rules.Responsibilities:You will manage the daily safety operations for our offices and factory floors while guiding a team of supervisors. Your main duties will include running safety training, set
We are looking for an EHS Manager to lead our safety and environmental programs at our manufacturing facility in Salt Lake City, Utah. In this role, you will lead a team to make sure our workplace stays safe, healthy, and up to date with all state and government rules.Responsibilities:You will manage the daily safety operations for our offices and factory floors while guiding a team of supervisors. Your main duties will include running safety training, set
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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