Clinical Research Coordinator

ICON; Madrid; Presencial; EUR 32.000 - 42.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Descripción de la vacante

ICON plc is seeking a Clinical Research Coordinator (50% FTE) in Valencia, Spain. You will coordinate day-to-day activities of clinical trials, ensuring execution and compliance with study protocols and regulatory standards.

You will manage trial logistics, support site staff, monitor progress, and maintain high data quality while upholding GCP guidelines and patient safety throughout the trial lifecycle.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Coordinator with understanding of trial processes and regulatory requirements.
• Strong organizational and multitasking skills to manage multiple trial aspects.

Responsabilidades

• Coordinate and manage the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics.
• Ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Monitor and document trial progress, including data collection, safety reporting, and regulatory compliance.
• Provide training and support to site staff to ensure effective execution of trial procedures and protocols.
• Build and maintain relationships with study participants and site personnel to facilitate smooth trial operations.

Conocimientos

Excellent communication

Organization & multitasking

Attention to data management

Team collaboration

Educación

Bachelor's degree in a relevant scientific discipline

Descripción del empleo

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.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request Here