We are seeking a detail-oriented, hands-on Production Associate to join our team. In this role, you will be involved in the full production cycle-from setting up and starting machine builds to material handling, machine turning, and post-processing part breakouts.This role operates in a hands-on manufacturing environment. Candidates should be comfortable working in a slightly dirty environment and ready to get their hands on the equipment every day.Respons
We are seeking a detail-oriented, hands-on Production Associate to join our team. In this role, you will be involved in the full production cycle-from setting up and starting machine builds to material handling, machine turning, and post-processing part breakouts.This role operates in a hands-on manufacturing environment. Candidates should be comfortable working in a slightly dirty environment and ready to get their hands on the equipment every day.Respons
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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