Clinical Research Coordinator

Responsibilities

• Assisting in the development and implementation of project plans to meet organizational goals.
• Collaborating with team members to identify opportunities for improvement and innovation.
• Gathering and analyzing data to provide insights that support decision-making processes.
• Contributing to the creation of reports and documentation to track project progress.
• Building strong relationships with colleagues to enhance teamwork and communication across functions.
• Your Profile:
• Bachelor's degree in a relevant field such as business administration, project management, or a related discipline.
• Experience in a similar role or environment, with a focus on project support.
• Experience in oncology therapeutic area strongly preferred.
• Strong analytical skills and attention to detail, with the ability to work effectively in a team.
• Excellent communication and interpersonal skills, with a collaborative approach to problem-solving.
• Proficiency in relevant software applications and tools to support project execution.
• #LI-JJ1
• 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

Benefits

Additional Information

Clinical Research Coordinator (contingent workers) 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. We are currently seeking a Clinical Research Coordinator to join our diverse and dynamic team. As the Clinical Research Coordinator at ICON, you will play a crucial role in supporting project initiatives and contributing to the overall success of our operations. You will assist in the execution of key tasks and collaborate with various teams to ensure alignment with organizational objectives. Locations: Warsaw, Gdańsk, Łódź Part-time, Site-based positions

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