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Clinical Research Coordinator

Remote, València·Part-time·Added yesterday (last checked 30 Oct)

ICON plc

60 open roles

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Our summary

Work mode: Remote, with limits
Contract: Fixed-term, part-time hours
Education: University degree
Benefits: Private health insurance, life insurance, gym access

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Skills

Requirements

What we're looking for

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.

Pay & benefits

What you'll get

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.

The role

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.

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'll 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.

About ICON plc

ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.

Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.

Industry: Clinical research
Headquarters: Dublin, Ireland

In their own words

Additional information

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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