Senior Crc Nurse

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

Visit our

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to read more about the benefits ICON offers.