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Job Purpose/ Summary: The Senior Clinical Project Manager 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 Senior CPM 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 Senior CPM 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 closeout 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 ICHGCP, regulatory requirements, trial procedures, and contracted scope.
• Develop and maintain trial timelines, deliverables, resources, plans and budgets to ensure timely and highquality execution.
• Serve as the primary operationallevel 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 trialassigned Director as appropriate.

• Assess, mitigate, and proactively communicate trial risks and issues, driving timely action plans to support delivery of key milestones and quality expectations.

• Ensure inspectionreadiness 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
• Graduate degree preferred
• Previous technical and managerial experience in conducting clinical pharmaceutical research studies at a CRO, in a hospital setting, or pharmaceutical company.
• Previous CRA experience preferred
• Experience or education indicating knowledge of medical and pharmaceutical terminology preferred
• Previous experience in a Clinical Project Manager level position preferred

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com 

Why CTI?

• Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
• Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note

• We will never communicate with you directly via Microsoft Teams Messaging or by text message
• We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Veterans/Disabled