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
We are seeking a high-energy, ambitious, and metric-driven Entry Level Full Desk Recruiter to manage the complete recruitment life cycle-from prospecting new client accounts to sourcing, interviewing, and placing top-tier talent. In this role, you will act as both a Business Development Manager and a Recruiting Specialist, building relationships with clients while delivering exceptional candidates to fill their hiring needs.Responsibilities:Business Develo
We are seeking a high-energy, ambitious, and metric-driven Entry Level Full Desk Recruiter to manage the complete recruitment life cycle-from prospecting new client accounts to sourcing, interviewing, and placing top-tier talent. In this role, you will act as both a Business Development Manager and a Recruiting Specialist, building relationships with clients while delivering exceptional candidates to fill their hiring needs.Responsibilities:Business Develo
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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