Project Manager, Accellacare - United Kingdom (Homebased)
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.

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

We have an incredible opportunity for a Project Manager to join ICON's Accellacare team. The Project Manager is responsible for the overall direction, coordination, implementation, execution, control and completion of single service global projects within the Accellacare network, ensuring consistency with ICON SOPs, study contracts, and budgets.

Location: United Kingdom (Homebased)

What you will be doing:

• Lead and manage the planning, execution, and monitoring of single service projects within the Accellacare program, ensuring adherence to project timelines, budgets, and quality standards
• Define project scope, goals, deliverables, and resource requirements
• Develop detailed project plans, timelines, and risk mitigation strategies
• Assemble, coordinate, and support project teams to ensure successful delivery
• Monitor project progress, quality, and budget using appropriate tools
• Communicate regularly with stakeholders through progress reports and updates, and collaborate with cross-functional teams to identify and address project risks and issues
• Manage project changes, conduct evaluations, and assess final outcomes

Your profile:

• Must have experience at a clinical research site as a site support coordinator, site activation, site partner, project support coordinator
• Must have previous experience with clinical trials project management
• Must have previous experience with clinical trials timeline and budget management
• Assertive and confident in communication, with the ability to lead discussions, set clear expectations, and address issues directly - face to face site negotiation
• Time management skills with the ability to prioritize efficiently
• Proactive mindset with strong critical thinking abilities to identify issues early and make sound, data-driven decisions
• Detail-oriented with a focus on accuracy, thoroughness, and consistency
• Must have Fluent English Communication, Writing and Reading
• Bachelor's degree, preferably in life sciences

#LI-SA2 #LI-Accellacare #LI-Onsite

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