Clinical Trial Manager

Responsibilities Demonstrated ability to manage CROs, vendors, study timelines, risks, action items, and cross-functional deliverables. Ability to identify issues, evaluate options, make sound recommendations, and drive timely resolution. Strong verbal, written, organizational, and interpersonal communication skills. Ability to manage competing priorities, work independently, and collaborate effectively with internal and external stakeholders. Experience using clinical systems and tools such as CTMS, eTMF, EDC, Microsoft Office, and study-specific tracking tools. Qualifications Bachelor’s degree in a life science, health-related, or related field preferred; equivalent directly related experience may be considered. At least eight years of clinical research experience, including at least two years of experience in clinical study management, clinical operations, or related clinical trial roles. Experience working with CROs, vendors, clinical sites, and cross-functional study teams is required. Experience in sponsor-side study management, vendor oversight, TMF management, audit/inspection readiness, and clinical study documentation is preferred. #J-18808-Ljbffr Intellectt Inc