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.

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.

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