Job Description
APX are partnered with a fast growing mid-sized CRO who are looking for a Senior Clinical Project Manager to lead a global study in Ophthalmology and support on an Oncology program. This is a hands on role where you have the opportunity to manage a pivotal trial from initiation through to close out whilst having the opportunity to grow a team of CRAs. Key Responsibilities Lead cross-functional project teams (Clinical Operations, Data Management, Biostats, Pharmacovigilance, etc.) to execute the project according to the contract and protocol. Develop and maintain essential project management documentation, including the Project Management Plan, Project Schedule, and Risk Management Plan. Proactively identify risks and implement mitigation strategies to keep projects on track. Oversee site selection, initiation, monitoring, and closeout phases. Client & Stakeholder Management Serve as the primary liaison between the CRO and the Sponsor, building trust and ensuring high levels of client satisfaction. Lead client meetings and present project status updates, including key metrics and performance indicators. Manage scope changes effectively, utilizing the Change Order process to protect the CRO’s profitability. Financial & Resource Management Manage project budgets, track actuals against forecasts, and ensure optimal resource allocation. Review and approve invoices, timesheets, and vendor contracts related to the project. Support the Business Development team in proposal development (budgeting and timeline strategy) for new opportunities. Leadership & Process Improvement Mentor and provide guidance to Clinical Research Associates. Contribute to the development and refinement of departmental SOPs and best practices. Qualifications Education & Experience Bachelor’s degree in Life Sciences, Nursing, or related field. Advanced degree preferred. Minimum 5-7 years of clinical research experience, with at least 3-4 years of dedicated Project Management experience within a CRO environment . Proven track record of successfully managing global or multinational Phase II-III trials. Must have experience with Ophthalmology and Oncology.