Job Description
📋 Description Develops/maintains project timelines from startup to completion. Drives development and distribution of study documents and tools. Manages regulatory documentation and audit readiness at sites and HQ. Negotiates study budgets with sites, Core Labs, and vendors. Attends site visits (initiation, monitoring, close-out). Leads complex US/OUS clinical projects; monitors progress and data. 🎯 Requirements Bachelor's in Biological Sciences or related field; 7+ years. 7+ years of relevant clinical trial experience. PM experience: at least 1 clinical project and 1 multicenter US/OUS trial. Proficiency with MS Project, MS Office, EDC Systems, and vendor oversight. Familiar with CFR and GCP/ICH requirements; medical terminology. Excellent communication and organizational skills; English fluency. 🎁 Benefits Collaborative, learning-focused team. Opportunity to contribute to innovative therapies. Generous benefits: medical, dental, vision, life. 401(k) with employer match; parental leave. Paid holidays and vacation; sick time.
