Note: The job is a remote job and is open to candidates in USA. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization focused on advancing treatments for critically ill patient populations. The Clinical Project Manager III is responsible for the execution and oversight of assigned clinical trials to ensure client goals of time, cost, and quality performance are met, often functioning as a global lead for trial operations.

Responsibilities

• 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

Skills

• 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 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

Benefits

• $15K sign-on bonus being offered!
• 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.
• 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.

Company Overview