Impress employers and recruiters.
Choose from hundreds of resume examples.
Impress employers and recruiters.
Choose from hundreds of resume examples.
Tailor your resume to this Project Manager, Accellacare role.
Rezi rewrites your resume against ICON plc's job description. Free.
Tailor your resume to this Project Manager, Accellacare role.
Rezi rewrites your resume against ICON plc's job description. Free.
Don't guess if your resume is good enough.
See how it scores against the Project Manager, Accellacare posting at ICON plc — free, in seconds.
Don't guess if your resume is good enough.
See how it scores against the Project Manager, Accellacare posting at ICON plc — free, in seconds.
About the Role
Accellacare, part of ICON's clinical research network, is seeking a Project Manager to transform the clinical trial experience for patients and sponsors. This role 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.
Responsibilities
- 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
- Collaborate with cross-functional teams to identify and address project risks and issues
- Manage project changes, conduct evaluations, and assess final outcomes
Requirements
- Must have experience at a clinical research site as a site support coordinator, site activation, site partner, or 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
- Fluent English Communication, Writing and Reading
- Bachelor’s degree, preferably in life sciences
- Must have the legal right to work in the country where the role is based
Skills
- Project Management
- Clinical Trials
- Timeline Management
- Budget Management
- Communication
- Negotiation
- Time Management
- Critical Thinking
- Attention to Detail
Location
- United Kingdom
Work Type
- Homebased
Education Level
- Bachelor’s degree
Benefits
- 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
About the Company
- 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.
Equal Opportunity
- 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.