Clinical Research Coordinator

Clinical Research Coordinator

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.

Part-time position (50% FTE)

Location: Valencia, Spain

As a Clinical Research Coordinator at ICON Plc, you will coordinate and manage the day-to-day activities of clinical trials to ensure efficient execution and compliance with study protocols and regulatory standards.

What You Will Do:

You will take ownership of clinical coordination deliverables, applying your expertise to complex challenges.

Key responsibilities include:

• Coordinating and managing the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics.
• Ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial.
• Monitoring and documenting trial progress, including data collection, safety reporting, and regulatory compliance.
• Providing training and support to site staff to ensure the effective execution of trial procedures and protocols.
• Building and maintaining strong relationships with study participants and site personnel to facilitate smooth trial operations and address any issues that arise.

Your Profile:

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Coordinator, with a comprehensive understanding of clinical trial processes and regulatory requirements.
• Strong organizational and multitasking skills, with the ability to manage multiple aspects of clinical trials simultaneously.
• Proficiency in clinical trial software and tools, with a keen eye for detail and accuracy in data management and documentation.
• Excellent communication, interpersonal, and problem-solving skills, with the ability to work effectively with a diverse team and drive successful trial outcomes.

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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