Senior Project Manager - Clinical Trials

📋 Description

• • Are you a seasoned Senior Project Manager with a deep understanding of full-service clinical trial management, particularly within the challenging and rapidly evolving field of Oncology?
• • Do you possess a genuine passion for contributing to the advancement of novel compounds and making a tangible impact on the health and lives of patients globally?
• • Do you approach clinical trial management with a consultative mindset, consistently proving yourself as an invaluable partner in operational delivery and strategic execution?
• • Precision for Medicine is actively seeking to expand our global team by hiring a Senior Project Manager, ideally with a strong background in Oncology, who has successfully managed full-service clinical trials within a Contract Research Organization (CRO) setting.
• • In this critical and influential role, you will assume comprehensive oversight for 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 Central Nervous System (CNS) trials will also be considered. You will be accountable for the end-to-end delivery of clinical projects, providing robust oversight to all functional departments involved, and rigorously ensuring that agreed-upon timelines, scope, budget, and quality standards are consistently met and exceeded.
• • Your responsibilities will encompass every stage of the study lifecycle. This includes active involvement in proposal strategy development, meticulous costing, and compelling bid defenses. You will guide studies through their full cycle to successful completion, cultivating and maintaining strong client relationships, effectively managing the project team, and diligently overseeing the budget and timelines throughout the entire duration of the trial.
• • You will operate as a key member of a dynamic cross-functional team, collaborating closely with both internal departments and external stakeholders. Your leadership will be instrumental in driving quality initiatives and coordinating the efforts of the entire study team to achieve project milestones.
• • We pride ourselves on fostering an amazing, high-energy, dedicated, and collaborative team environment. Our team members genuinely enjoy tackling complex challenges, thrive on meticulous attention to detail, and flourish in dynamic, fast-paced settings. If you are someone who naturally takes charge, seeks out positive teamwork to achieve extraordinary results, and is eager to contribute to groundbreaking research, then this opportunity is tailor-made for you.
• • How we will support your professional growth and keep you engaged:
• • You will independently lead and manage clinical projects, ensuring adherence to the study budget and scope of work. Leveraging your strong interpersonal and organizational skills, you will set and achieve ambitious objectives in project execution, encompassing both contracted deliverables and financial targets. The opportunity to manage international trials will also be a key aspect of this role.
• • You will serve as the primary point-of-contact and liaison with our clients, delivering exceptional customer service. This includes active participation in proposal development activities and presenting to clients.
• • You will liaise effectively with the Project Team and senior management at both Precision for Medicine and our sponsor organizations, including C-level executives.
• • You will expertly handle and lead all facets of clinical research trials, ensuring seamless operations.
• • You will provide total project management across all functional areas, including but not limited to data management, safety monitoring, clinical operations, medical monitoring, and biostatistics.
• • You will prepare and deliver comprehensive project status updates for clients and internal management, clearly identifying key deliverables, performance metrics for success, and any necessary escalations.
• • You will act as a proactive and engaged member of the Project Team, contributing significantly to the efficient management and successful execution of trials.
• • You will prepare and review essential study documentation, such as protocols, project plans, informed consent forms, site contracts, and budgets, ensuring accuracy and compliance.