Clinical Project Manager **Level Dependent on Experience**

Clinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization focused on advancing treatments for chronically and critically ill patients. We support clinical research throughout the life cycle of development, from drug concept to commercialization. Responsibilities Plan, implement, evaluate, and complete full execution of assigned clinical trials, often acting as global trial lead. Set goals, timelines, and provide oversight and positive leadership to motivate the team to achieve high‑quality outcomes. Coordinate operational aspects to ensure compliance with ICH guidelines, Good Clinical Practice, and regulatory requirements. Manage full‑scope clinical trial projects, including global trials from start‑up through analysis phase, and oversee functionally assigned team members. Control project budget, assess profit margins, and collaborate with trial‑assigned directors to maintain budget alignment. Prepare, review, and update trial plans, timelines, schedules, resources, and budgets. Maintain clear communication with vendors, ensuring timely delivery and financial oversight. Oversee Clinical Research Associate (CRA) activities, including site monitoring and data review. Lead client and team meetings, ensuring documentation of decisions and outcomes. Provide oversight of the Clinical Trial Master File (TMF) to ensure compliance and completeness. Participate in business‑development activities and process‑improvement initiatives. Mentor other CPM staff. Regionally Specific Essential Functions Europe: Preparation and negotiation of site budgets, site payments, and payment of site invoices handled by the EU Clinical Trial Budget Management Team with assistance of regional CRAs or Study Start‑up Specialists. LATAM: Provide expertise and support for country‑specific regulations and submissions. Conduct regional feasibility activities for trial and RWE work. Conduct RWE activities as needed in the region. Provide Importer of Record services as needed. MEA: Provide expertise and support for country‑specific regulations and submissions. Conduct regional feasibility activities and RWE work. APAC: Provide expertise and support for country‑specific regulations and submissions. Conduct regional feasibility activities and RWE work. What You’ll Bring Bachelor’s degree in allied health (e.g., nursing, pharmacy, health science) with clinical trial management experience or equivalent education and work experience. Minimum 6 years of clinical research experience (CRO CRA, research manager, or similar). Project‑management experience in a clinical setting is acceptable. Graduate degree preferred. At least 5 years of experience focused on rare disease, oncology, cell‑gene therapy, or transplant. Experience as a Clinical Project Manager or Clinical Trial Manager preferred. Eligibility to live and work in Argentina, Brazil, or Mexico. Why CTI? Advance your career through a structured mentoring program and leadership courses. Work in an award‑winning, collaborative culture with hybrid work options. Make a lasting impact by advancing treatments for critically ill patients. Important Note We use a secure email domain @ctifacts.com for any direct communication during the hiring process. Applications should be submitted directly through our website or verified LinkedIn page. Hiring Safeguards – We will never contact you via Microsoft Teams, text message, or ask for bank‑account information during recruitment. Referrals increase your chances of interviewing at CTI by 2×. #J-18808-Ljbffr