Clinical Research Nurse I

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government, and public health organizationsThat’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and are the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Title: Clinical Research Nurse

Job Type: PRN

Summary: As part of the clinical trial research team, the Clinical Research Nurse will have responsibility for the delivery of direct and indirect care for research studies undertaken in the clinical research unit, in accordance with the ICON standard operating procedures, the clinical trial protocol, Food and Drug Administration, Good Clinical Practice, International Conference on Harmonization Good Clinical Practice Guidelines and the Clinical Trials Directive, Medicines for Human Use Act Statute No 1928 as appropriate.This position participates in the effective running of research studies on a day-to-day basis maintaining the confidentiality, safety and well being of study participants and utilizing skill knowledge and judgement to provide a high standard of care while maintaining dignity and respect at all times.

Duties:

Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance. As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.• Travel (approximately 0%) domestic and/or international.• Ensure volunteer safety and well being in a variety of settings working collaboratively within a multidisciplinary team. Identify and report any potential or actual adverse events to a senior nurse and physician in a timely manner.• Perform all types of drug administration for which they have been competency assessed in accordance with the study protocol and within the appropriate guidelines for the administration of medicines.• To be competent in performing and supervising other members of the multidisciplinary team in core clinical skills, utilizing clinical knowledge to identify potential clinical abnormalities and recognizing and reporting any deviation from the parameters as stated in the study protocol.• To perform clinical procedures as per SOP/protocol including but not limited to;• Recording of 12 lead ECG• Continuous Cardiac Monitoring• Blood sampling both direct Venipuncture and via cannula• Recording of vital signs in accordance with the study protocol• Pulse Oximetry• Collect accurate high quality data in accordance with Good Clinical Practice and resolve queries in a timely manner so as not to delay time to study completion.• May screen participants for inclusion into study, based on predetermined criteria.• May collect medical history and questionnaires. Evaluate and interpret collected data.• May assist principal investigator and other members of the research team in the development of plans and protocols for clinical research studies and contribute to the analysis and interpretation of results as appropriate.• Provide basic nursing care and treatment as requested by the physician.• Undertake quality control check of assigned protocols and relevant study documentation and provide feedback to the Project Manager or designee in a timely manner.• Demonstrate and share knowledge and understanding of the research process, the volunteer process and study flow within the clinical unit.• Participate in internal and external clinical trial meetings and trainings as applicable.• Quality check all completed source documents to ensure accuracy, legibility and completion of all data points.• To be proactive in developing and implementing quality initiatives within the clinical area providing prompt feedback on procedural audit reports and attendance at the Quality Forums.• Continuously update knowledge through self development and participation in learning activities. Maintain an up-to-date training record and utilize evidence- based nursing.• Assist in training and mentoring of new clinical personnel.• Undertake sample handling and sample processing within the clinical preparation area as per protocol as required.• May act as shift lead when required, coordinating and organizing clinical staff efficiently in the absence of the Clinical Research Sister/Charge Nurse or designee.• To undertake other reasonably related duties as may be assigned from time to time.

Benefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON is an equal opportunity and inclusive employer and 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 through the form below.