As a Project Manager (Oncology) at ICON, you will be responsible for leading and coordinate project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards for our large pharmaceutical clients.

What You Will Do:

Your focus will be on coordinating project and program management delivery, resolving issues, and developing team capability.

Key responsibilities include:

• Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.

• Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.

• Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.

• Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organizational objectives.

• Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.

Your Profile:

You will have solid project and program management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

• Bachelor's degree in project management, business, or a related field is preferred, with significant experience in project management and team leadership.

• Proven track record of successfully managing projects from inception to completion, with a focus on delivering results within scope, time, and budget constraints.

• Strong leadership and organizational skills, with the ability to effectively manage project teams and prioritize tasks.

• Excellent communication and interpersonal skills, with the ability to build relationships and manage stakeholder expectations.

• Proficiency in project management tools and methodologies, with certifications such as PMP or PRINCE2 being advantageous.

• Detail-oriented, proactive, and adaptable, with a commitment to achieving project goals and driving continuous improvement.

• Must have at least 2 years of experience working in for a CRO supporting Oncology/Hematology clinical trials

• Radioligand experience highly preferred

• Willingness to travel as required (approximately 30%)

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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.

Visit our to read more about the benefits ICON offers.