Clinical Operations Manager - 246826

Get AI-powered advice on this job and more exclusive features. This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $90,000.00/yr - $110,000.00/yr Clinical Operations Manager Location: Seattle, WA (98104) Overview The Clinical Operations Manager is responsible for overseeing the daily operations and overall performance of the Clinical Operations team, ensuring compliance, efficiency, and high-quality execution of all clinical trials conducted at the site. This role provides leadership to the Clinical Research Coordinators (CRCs) and other operations staff, ensuring studies are conducted according to protocol, regulatory requirements, and site standards. Essential Job Functions Supervise Clinical Research Coordinators (CRCs), providing coaching, mentorship, performance feedback, and career development. Oversee and support the Assistant ClinOps Manager, who manages Research Assistants (RAs) and Laboratory Technicians. Lead team meetings, set clear expectations, and ensure accountability across all ClinOps functions. Foster collaboration between Clinical Operations, Recruitment, and other site departments. Operational Oversight Ensure trials are conducted in compliance with ICH-GCP, FDA regulations, IRB requirements, and site SOPs. Monitor workload distribution and study assignments for CRCs; adjust as needed to optimize efficiency and balance priorities. Identify and implement process improvements to streamline operations and enhance participant and sponsor satisfaction. Oversee internal audits and assist with sponsor, CRO, and FDA inspections to ensure site readiness at all times. Performance & Reporting Develop, track, and present ClinOps performance metrics (weekly, monthly, and annual) to site leadership. Monitor study timelines, enrollment progress, and data quality; proactively address barriers to success. Provide input on site capacity, staffing needs, and study feasibility to support business development. Study Management (as applicable) Serve as a lead coordinator on select clinical trials, ensuring protocol adherence, participant management, and data oversight. Contribute to the development of study-specific documents and processes (e.g., process flows, CRFs, training materials). Support recruitment and retention strategies by collaborating with recruitment staff and engaging directly in patient-facing activities as needed. Strategic & Cross-Functional Engagement Participate in site-level leadership meetings and annual strategy planning sessions. Provide input on study contracts, budgets, and operational considerations as requested by the executive team. Support hiring, onboarding, and training of new ClinOps staff, ensuring smooth integration and adherence to site standards. Qualifications Excellent communication, leadership, and organizational skills. Strong attention to detail, flexibility, and a collaborative mindset. Minimum of 3–5 years of experience in clinical research or equivalent (at leadership’s discretion). Minimum of 2–4 years of experience managing a team. Seniority level Mid-Senior level Employment type Full-time Job function Management and Research Industries Biotechnology Research and Research Services #J-18808-Ljbffr Medix™