ICON plc Healthcare/BioTech

Senior Clinical Project Manager

Remote Full-time

Location: US, Blue Bell (ICON)

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%).

#LI-MH1

#LI-REMOTE

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.
  • Are you a current ICON Employee? Please click here to apply

Job description provided by ICON plc.
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