Clinical Research Coordinator

What You Will Be Doing:

• 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.

• 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.

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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.