Project Manager

Study Delivery Support PM - UK

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Study Delivery Project Management Support

Oncology Clinical Research

Join a dynamic Oncology team supporting the delivery of complex global clinical studies that help bring innovative treatments to patients worldwide.

As a Study Delivery PM Support Specialist , you will work closely with study teams, CRO partners and key stakeholders to ensure studies are successfully delivered from start-up through to close-out. This is an excellent opportunity for someone with clinical research industry experience who enjoys a varied role with broad exposure to study operations and project management activities.

Key Responsibilities

Study Start-Up

• Support vendor procurement, contracting and purchase order processes.
• Assist with study budgets, study set-up and oversight documentation.
• Coordinate study documentation, action trackers and meeting minutes.
• Support study team and country-level communications.

Study Delivery

• Act as a key liaison between internal study teams and CRO project managers.
• Maintain study documentation, risk logs and tracking tools.
• Coordinate cross-functional meetings and stakeholder communications.
• Support study registration activities, site contracting and ethics approval processes.
• Assist with advisory board and steering committee meeting preparation and documentation.
• Provide support for investigator contracting, payments and study systems.

Study Close-Out

• Support study closure activities, including system close-out, archiving and final document management.

Ideal Candidate

• Bachelor's degree in a scientific or life sciences discipline.
• Strong experience working within the pharmaceutical, biotechnology, CRO or clinical research industry in an Oncology project management role.
• Home-based already residing in the UK.
• Experience of Phase IV and/or Real World Evidence trials in a trial management capacity.
• Proven ability to manage multiple priorities and projects simultaneously.
• Strong organisational, stakeholder management and communication skills.
• Experience working within cross-functional, matrix environments.

Why Apply?

• Contribute to innovative oncology research.
• Gain exposure to complex global clinical studies.
• Work with a broad range of internal and external stakeholders.
• Develop your project management and clinical operations expertise in a highly collaborative environment.

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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