Clinical Research Nurse
About the role
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ICON site network group is a rapidly expanding and dynamic fast track company dedicated to the recruitment and running of clinical trials at its own Research Centres.
We concentrate on quick patient recruitment, high data standards and delivering excellent patient experience resulting in a high level of patient retention. These qualities are what our Sponsors look for in a leading Dedicated Clinical Research Organisation and you can be part of our success story.
This is a great opportunity for a nurse with a keen interest in clinical trials to play an important role in the advancement of new treatments.
Role Responsibility
As a Research Nurse 1 or 2 you are required to participate in the creation and maintenance of a high-quality clinical research environment.
You will initiate and manage nursing activities related to clinical trials, from initiation to termination, per ICH/GCP guidelines and to ensure the commercial success of the centre by recruiting and maintaining optimum patient numbers.
Key Accountability:
· Complete all relevant clinical competency training assessments, and attend all relevant research study protocol training, and complete all mandatory training, per the COP's/SOP's.
· Perform all visits, observations, safety reporting and interventions with the participants in accordance with procedures and schedule of the study protocol, company SOP's and policies.
· Stay abreast of all relevant SOPs and regulatory guidance, performing all activities in compliance to these.
· Carry out PIVs efficiently and effectively to optimise patient recruitment.
· Encourage patients to continue within the study, and to participate in future trials.
· Collect, record, verify and enter study data into the source notes, CRF/eCRF, and all associated paperwork, with a high degree of accuracy.
· Ensure that all data queries are acted upon in a timely and efficient manner.
· Participates in site and investigator meetings when required.
· Initiates emergency action when required e.g. cardiac arrest, anaphylaxis management, fire, or critical incidents.
The Ideal Candidate
As a successful Research Nurse 1, you will likely have:
· Registration with no limitations to practice within the Nursing and Midwifery Council (Adult)
· Broad post-registration experience
· Some understanding of clinical research
· Well-developed interpersonal and communication skills
· Relevant clinical skills
· Strong motivation and an enthusiastic disposition
A successful applicant for the level 2 position will need previous experience working as a Research Nurse in a controlled medical testing environment.
What's Next?
Following your application, we will contact you and one of our dedicated recruiters will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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. Learn more about Our Culture at ICON
Day in the life
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12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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12/01/2025
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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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