[Hiring] Senior Clinical Project Manager @ICON plc

Role Description

As a Senior Project Manager at ICON, you will be responsible for leading full-service clinical research projects from study start-up through closeout, ensuring successful execution and delivery of project objectives. This role requires an experienced Project Lead with a strong background in oncology clinical trials, with radiopharmaceutical experience highly desired.

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.

• 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.

Qualifications

• 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%).

Benefits

• Competitive base salary and performance related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.
• Benefits may vary depending on role and location.