Sr CRC Nurse
About the role
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This is an exciting opportunity to join ICON
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.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer, including disability/veteran, and committed to providing a workplace free of discrimination and harassment.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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