Sr. Manager, Clinical Operations / Associate Director, Clinical Operations
- $140,000.00 to $160,000.00
- Las Vegas United States
Sr. Manager / Associate Director, Clinical Operations
Las Vegas, NV
On-site
Meet Life Sciences is representing a small CRO seeking a Sr. Manager, Clinical Operations or Associate Director, Clinical Operations to join its team in Las Vegas, Nevada. This individual will play a critical leadership role overseeing clinical operations within a dedicated Phase 1 clinical research unit, ensuring the successful execution of early-phase studies while leading and developing site-based operations staff.
This is an excellent opportunity for a clinical operations leader with deep Phase 1 experience, strong people management capabilities, and a hands-on approach to operational excellence in a fast-paced clinical research environment.
Key Responsibilities
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Provide operational leadership for a Phase 1 clinical research clinic, ensuring studies are conducted efficiently, compliantly, and in accordance with protocol, SOPs, GCP, and applicable regulatory requirements
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Oversee day-to-day clinical operations across early-phase studies, including study start-up, conduct, and closeout activities
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Directly manage, mentor, and develop clinical operations staff; previous experience managing individuals is required
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Drive staff performance, accountability, and professional development across the clinical operations function
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Partner cross-functionally with clinical, medical, regulatory, quality, and site leadership to ensure seamless study execution
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Ensure adequate staffing, training, and resource allocation to support study timelines and clinic throughput
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Monitor operational metrics, identify risks proactively, and implement solutions to support enrollment, protocol adherence, patient safety, and data quality
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Serve as a key point of escalation for operational issues within the clinic and provide leadership in resolving study or site-related challenges
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Support continuous improvement initiatives across clinic operations, workflows, SOPs, and overall site performance
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Help maintain inspection readiness and a culture of quality throughout the organization
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Collaborate with senior leadership on strategic planning, capacity management, and operational scaling as needed
Qualifications
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Bachelor’s degree required; advanced degree preferred
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7+ years of clinical operations experience, with title level depending on overall depth of experience and leadership background
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Extensive Phase 1 clinical trial experience is required
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Prior experience working within an early-phase clinical research unit, Phase 1 site, or CRO environment strongly preferred
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Previous people management experience is required, with demonstrated success leading, mentoring, and developing teams
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Strong understanding of GCP, ICH guidelines, SOPs, and regulatory requirements relevant to clinical trial conduct
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Proven ability to manage multiple studies, priorities, and operational demands in a dynamic clinical environment
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Strong communication, leadership, problem-solving, and organizational skills
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Ability to operate both strategically and hands-on when needed
Preferred Background
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Experience overseeing operations in a Phase 1 clinic or inpatient/outpatient early-phase setting
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Familiarity with healthy volunteer and/or patient-based early-phase studies
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Prior CRO experience and comfort working in a high-growth, entrepreneurial environment
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Experience supporting operational process improvement and clinic optimization initiatives