Senior Clinical Study Manager

Job not on LinkedIn

🔥 1 minute ago

🏄 California, Illinois – Remote

🏄 California – Remote 🌽 Illinois – Remote

💵 $116k - $170k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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Danaher Corporation

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Danaher Corporation is a leading global life sciences and diagnostics innovator that develops and supplies instruments, technologies, software, and services to accelerate scientific research, biotechnology development, and clinical diagnostics. The company operates through businesses focused on biotechnology tools, diagnostics platforms, and life sciences products, leveraging the Danaher Business System and an acquisition-driven strategy to scale technologies and support customers across academia, pharmaceutical and biotech companies, and clinical laboratories.

📋 Description

• Manage overall clinical execution of pre-clinical and clinical trials across a program • Lead end-to-end clinical trial execution from planning and site selection through enrollment, monitoring, and closeout • Ensure specimen and study-material readiness and accountability • Oversee clinical staff and coordinate sites, CROs, vendors, and external laboratories • Develop and maintain study documentation and oversight records • Ensure protocol compliance, traceability, inspection readiness, and risk and issue management • Manage clinical trial budgets, resources, timelines, and milestones • Track performance against plans and recommend adjustments • Partner with executive leadership and cross-functional teams to coordinate data review, study completion, decisions, and progress reporting • Provide oversight, supervision, and mentorship to associates assigned to the project

🎯 Requirements

• Bachelor’s degree in a scientific discipline or equivalent experience • 8+ years of clinical research experience in the medical device (IVD preferred), biotechnology, or pharmaceutical industries • Working knowledge of FDA regulatory requirements related to clinical research • Up to 20% travel • At least 3 years of clinical research associate (CRA) experience and 3 years of study management experience (plus) • Experience with in vitro diagnostic clinical trials (plus) • Experience with clinical trials in infectious diseases and/or oncology (plus)

🏖️ Benefits

• Bonus/incentive pay eligibility • Paid time off • Medical insurance • Dental insurance • Vision insurance • 401(k) • Flexible, remote working arrangements for eligible roles • Remote work from home • Career growth and development opportunities

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