Clinical Project Manager III

Job Purpose/ Summary The Clinical Project Manager III/ Senior is responsible for execution and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM III/ Senor is expected to be independent but may require consultation and guidance from the trial‑assigned Director to ensure successful clinical trial execution and to support other functional team members’ management of daily trial operations. Often functions as a global lead to provide client interface and oversight of trial regions’ operational activities. The CPM III/ Senior is seen as skilled in the application of the essential functions of the CPM role listed below. What You'll Do Manage the planning, implementation, execution, and close‑out of assigned clinical trials (Phase I–IV), often functioning as a global trial lead. Provide operational oversight and coordination across functional teams and regions to ensure adherence to ICH‑GCP, regulatory requirements, trial procedures, and contracted scope. Develop and maintain trial plans, timelines, deliverables, resources, and budgets to ensure timely and high‑quality execution. Serve as the primary operational‑level client contact, leading study meetings, preparing project status reports, and supporting effective communication and documentation. Monitor project performance including timelines, KPIs, scope, budget, and vendor deliverables, escalating risks and issues to the trial‑assigned Director as appropriate. Ensure inspection‑readiness through oversight of TMF completeness, CRA activities, site performance, and compliance with project and communication plans. What You'll Bring Bachelor’s degree in allied health fields such as nursing, pharmacy, health or natural sciences, preferably with clinical trial management experience or an equivalent combination of education and relevant work experience At least 6 years of clinical research experience (CRO CRA or Research Manager, Site Research Manager, Central Clinical Research Laboratory Manager) or possesses transferrable skills and experience in project management in a clinical setting or relatable industry Previous technical and managerial experience in conducting clinical pharmaceutical research studies in a hospital setting, a pharmaceutical company, or CRO. Previous CRA experience preferred Experience or education indicating knowledge of medical and pharmaceutical terminology preferred Previous experience in a Clinical Project Manager or Clinical Trial Manager level position preferred Equal Opportunity Employer/Veterans/Disabled Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr