3 days ago
🏢 In-office - Bay Area
• Independently manage all clinical aspects of small to medium-sized studies • Liaise with cross-functional teams to ensure protocol compliance • Implement and monitor study activities according to GCPs and SOPs • Develop study processes and support documentation • Participate in recruitment of Investigators • Conduct oversight visits and ensure regulatory compliance • Maintain Trial Master File and regulatory documents
• BA/BS degree in relevant field, nursing degree, or equivalent experience • 4+ years of experience in clinical research for a Sponsor company, CRA/field monitor, or CRO setting
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