Senior Clinical Project Manager

Regulatory Jobs; United States; Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive base salary and incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and开发

Learning and development opportunities

Job summary

ICON is seeking a Senior Clinical Project Manager to lead full-service oncology trials with radiopharmaceutical experience preferred. This remote-US role requires strong cross-functional leadership, plan development, and stakeholder communication.

You will oversee study start-up through closeout, mentor teams, and ensure delivery of project objectives while applying industry best practices and emerging technologies.

Qualifications

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
• Extensive clinical research project management experience within the pharmaceutical/biotech/CRO landscape.
• Demonstrated experience as the overall Project Lead coordinating cross-functional areas from start-up to closeout.
• Strong oncology clinical trial experience.
• Radiopharmaceutical/radioligand trial experience is highly desired.
• Strong proficiency with project management methodologies and attention to detail.
• Excellent communication and leadership skills; ability to mentor teams.

Responsibilities

• Lead full-service clinical trials from start-up to closeout.
• Develop and execute project plans, timelines, and deliverables.
• Coordinate cross-functional activities across study start-up, conduct, and closeout.
• Mentor team members and drive a culture of excellence.
• Present findings and project status to stakeholders with clear reporting.
• Stay current with industry trends and radiopharmaceutical strategies.

Skills

Project leadership

Cross-functional teams

Oncology clinical trials

Radiopharmaceutical experience

Communication skills

Analytical skills

Problem-solving

Mentoring

Attention to detail

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Project management tools

Job description

Senior Clinical Project Manager - Remote, US

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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.

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%).

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 careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.