Senior Project Manager - Clinical Trials

📋 Description

• • Are you a seasoned full-service Project Manager with a deep understanding of clinical trials, driven by the ambition to overcome the complex challenges in the research and development of novel compounds, particularly in Oncology?
• • Do you possess a genuine passion for making a tangible impact on the health and lives of patients globally, and do you approach trial management with a consultative mindset, acting as an invaluable partner in operational delivery?
• • Precision for Medicine is actively seeking a Senior Project Manager, ideally with a strong background in Oncology, to join our dynamic global team. We are looking for individuals who have successfully managed full-service clinical trials within a Contract Research Organization (CRO) setting.
• • In this critical role, you will be entrusted with comprehensive oversight of clinical projects, spanning Phase I-IV trials across global and regional landscapes. Your expertise will be particularly valued in Oncology, though experience in Rare Diseases or CNS is also highly regarded.
• • You will hold ultimate accountability for the successful delivery of clinical projects, ensuring meticulous oversight of all functional departments involved. Your focus will be on consistently meeting agreed-upon timelines, scope, budget, and quality standards.
• • Your involvement will encompass every stage of the study lifecycle, from the initial proposal strategy, development, and costing, through to the crucial bid defense process. You will guide studies from inception to completion, expertly managing client relationships, project teams, budgets, and timelines throughout.
• • You will collaborate within a cross-functional team, engaging effectively with both internal and external stakeholders. A key aspect of your role will be to drive quality initiatives and provide coordinated leadership to the study team.
• • We pride ourselves on fostering an amazing, high-energy, dedicated, and collaborative team environment. Our team members thrive on challenges, excel in managing intricate details, and flourish in dynamic settings. If you are someone who naturally takes charge, seeks out positive teamwork, and is committed to delivering extraordinary results, this opportunity is tailor-made for you.
• • Your responsibilities will include independently leading clinical projects, ensuring strict adherence to study budgets and the defined scope of work. You will leverage your exceptional interpersonal and organizational skills to establish and achieve project objectives, encompassing both contracted deliverables and financial targets. The scope of your work may extend to managing international trials.
• • You will serve as the primary point of contact and liaison with clients, delivering outstanding customer service. This includes active participation in proposal development activities and client presentations, showcasing your strategic thinking and communication abilities.
• • You will engage in crucial liaisons with Project Teams and senior management at both Precision Medicine Group and sponsor organizations, including C-level executives, fostering strong collaborative relationships.
• • You will be responsible for handling and leading all facets of clinical research trials, ensuring seamless execution from start to finish.
• • Your role will involve total project management across all functional areas, including but not limited to data management, safety monitoring, clinical operations, medical monitoring, and biostatistics, ensuring integrated and efficient project progression.
• • You will be tasked with preparing and presenting comprehensive project status updates to clients and internal management. This involves clearly identifying key deliverables, defining performance metrics for success, and proactively managing any escalations.
• • You will act as an integral and active member of the Project Team, contributing significantly to the efficient management and successful execution of trials.
• • You will be responsible for preparing and reviewing essential study documentation, such as protocols, detailed project plans, informed consent forms, site contracts, and budgets, ensuring accuracy and compliance.