Associate Director Clinical Operations at Meet

180000 USD - 180000 USD South San Francisco, United StatesPermanentJob Title: Associate Director, Clinical OperationsLocation: South San Francisco, CA (Onsite 3 days per week)Job Type: Full-timePosition Summary:Our client is seeking an experienced and driven Associate Director of Clinical Operations to lead our global Phase 3 clinical trials. The successful candidate will have substantial experience in managing Phase 3 studies, a proven track record as an independent study lead for at least 3 years, and ideally some experience in people management. This role requires a strategic leader who excels in operational excellence and team collaboration to ensure the successful execution of clinical trials.Key Responsibilities:Oversee and manage global Phase 3 clinical trials, ensuring compliance with regulatory requirements, study protocols, and project timelines.Act as the primary study lead, independently managing all facets of trial execution, including protocol development, site management, and data collection.Collaborate closely with cross-functional teams, including Clinical Development, Data Management, Regulatory Affairs, and Medical Affairs, to ensure alignment and successful trial outcomes.Provide leadership and guidance to study teams, including mentoring and managing staff to enhance team performance and development.Develop and maintain strong relationships with key stakeholders, including external vendors, clinical sites, and regulatory bodies.Monitor trial progress, identify potential risks, and implement corrective actions to ensure timely and efficient study completion.Prepare and present regular updates and reports to senior management and other key stakeholders.Qualifications:Bachelor's degree in Life Sciences or a related field; advanced degree (e.g., Master’s, Ph.D.) preferred.At least 7 years of experience in clinical operations, with a strong focus on global Phase 3 studies.Demonstrated experience as an independent study lead for a minimum of 3 years, with a proven ability to manage complex trials effectively.Prior experience in a people management or leadership role is highly desirable.In-depth knowledge of clinical trial design, regulatory guidelines, and industry best practices.Exceptional organizational, communication, and problem-solving skills.Ability to work onsite in South San Francisco 3 days per week.Apply for full job description and company details!