Senior Clinical Project Manager

What You Will Do: You will manage day-to-day project and programme management activities, supporting cross-functional teams to deliver quality outcomes. As the overall Project Lead, you will have end-to-end accountability for full-service studies, coordinating multiple functional areas and serving as a key point of contact throughout the lifecycle of the project.

Key responsibilities include: Developing and executing project plans, focusing on achieving project goals and objectives across full-service clinical trials. Providing end-to-end project leadership across study start-up, conduct, and closeout, coordinating cross-functional clinical research activities and deliverables. Leading cross-functional teams to ensure the successful implementation of project activities and alignment against project timelines, objectives, and commitments. Collaborating with stakeholders to identify project requirements, define project scope, and maintain alignment throughout the project lifecycle. Leading complex oncology studies, with the ability to apply relevant oncology and radiopharmaceutical clinical research experience to project execution. Mentoring and guiding team members, fostering a culture of excellence and continuous improvement. Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner. Staying abreast of industry trends and emerging technologies to integrate best practices into project management strategies. Contributing to organizational growth through effective project leadership and strategic planning.

Your Profile: You will have significant experience serving as the Project Lead/Project Manager for full-service clinical trials, with demonstrated ability to lead cross-functional teams and maintain oversight across the full study lifecycle. Strong oncology experience is required, and previous experience supporting radiopharmaceutical clinical trials is highly desired. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field. Extensive clinical research project management experience within the pharmaceutical, biotechnology, or CRO industry, including direct experience leading full-service clinical trials. Demonstrated experience as the overall Project Lead with responsibility for coordinating multiple functional areas and driving successful delivery of studies from start-up through closeout. Strong oncology clinical trial experience. Experience with radiopharmaceutical/radioligand clinical trials is highly desired. Strong proficiency in project management tools and methodologies, with excellent attention to detail. Excellent analytical and problem-solving skills, with the ability to develop effective project strategies. Demonstrated leadership skills, with experience managing and mentoring cross-functional teams effectively. Exceptional communication skills, with the ability to convey technical concepts to diverse audiences. Detail-oriented, with strong organizational skills to manage multiple priorities and deadlines in a dynamic environment. Willingness to travel as required (approximately 25%).