Senior Clinical Project Manager

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.

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%).

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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.

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