Senior Oncology PM - Remote Radiopharma Focus

ICON; Center Square (PA); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Job summary

ICON is seeking a Senior Clinical Project Manager (Oncology/Hematology) for a United States - Remote role. You will manage end-to-end clinical projects, focusing on radiopharmaceutical and radioligand studies, while leading cross-functional teams and mentoring staff.

You will work with stakeholders to define scope, deliverables, and milestones, ensuring high quality outcomes in a fast-paced, regulated environment. A strong oncology background and travel readiness (about 25%) are required.

Qualifications

• Bachelor's degree in a relevant scientific or healthcare field.
• Proven track record leading CRO projects in oncology.
• Experience with radiopharmaceuticals or radioligand therapies preferred.
• Strong communication and leadership capabilities.
• Detail-oriented with excellent problem-solving skills.

Responsibilities

• Manage day-to-day clinical project management activities to meet objectives.
• Lead cross-functional teams across oncology programs.
• Collaborate with stakeholders to define project scope and requirements.
• Mentor and guide junior staff and foster a culture of excellence.
• Develop and present project documentation and reports for stakeholders.
• Stay current with industry trends to inform management strategies.
• Travel approximately 25% as required.

Skills

Clinical project management

Leadership

Analytical skills

Communication

Attention to detail

PM tools

Education

Bachelor's degree in a relevant scientific field

Tools

Project management tools

Job description

ICON is seeking a Senior Clinical Project Manager (Oncology/Hematology) for a United States - Remote role. You will manage end-to-end clinical projects, focusing on radiopharmaceutical and radioligand studies, while leading cross-functional teams and mentoring staff.

You will work with stakeholders to define scope, deliverables, and milestones, ensuring high quality outcomes in a fast-paced, regulated environment. A strong oncology background and travel readiness (about 25%) are required.