Senior CRC Nurse
- Madrid
- ICON Full Service & Corporate Support
- Clinical Research In-Home Services, Nurse
- Office Based
Talent Acquisition Coordinator
- Full Service Division
About the role
Senior CRC Nurse - Madrid, Spain.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
ICON is currently seeking a Senior Clinical Research Coordinator Nurse to join our diverse and dynamic team. As a Senior CRC Nurse at ICON Plc, you will play a vital role in managing and coordinating clinical trial activities with a focus on patient care and safety. You will contribute to the success of clinical trials by overseeing participant recruitment, monitoring, and ensuring adherence to study protocols and regulatory standards.
What You Will Be Doing:
Clinical Trial Coordination:
Manage the daily operations of assigned clinical trials in accordance with ICH-GCP, protocol requirements, and ICON/Accellacare SOPs
Act as the primary liaison between the site, sponsor, and study participants
Ensure timely and accurate documentation, data collection, and reporting
Support regulatory and ethics submissions as needed
Nursing & Patient Care Duties:
Perform clinical assessments including vital signs, ECGs, and medical history evaluations
Administer study-related procedures such as venepuncture, cannulation, and sample collection
Monitor and support patient safety and well-being throughout the trial
Educate participants on study requirements, procedures, and informed consent
Respond to and report adverse events in line with protocol and safety guidelines
Required Qualifications & Experience:
Registered Nurse (RN) with valid and active registration
Professional level of English – both written and spoken
Prior experience working as a Clinical Research Nurse or Study Coordinator within a clinical research environment
Strong understanding of ICH-GCP and trial protocols
Preferred Skills:
Certified and experienced in venepuncture and cannulation
Strong attention to detail, organisation, and time management
A compassionate and patient-centred approach to care
Comfortable working in a fast-paced, multi-study environment.
#LI-LP1
This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
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
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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