Clinical Research Nurse I
ICON, San Antonio, TX, United States
JR148520 Clinical Research Nurse I
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.
The Role
As a key member of the clinical unit team, you will support the delivery of clinical trials by ensuring the safety, wellbeing, and accurate monitoring of study participants in both inpatient and outpatient/ambulatory settings, including screening visits. You will work collaboratively with physicians, investigators, and study staff to ensure protocol adherence and high-quality data collection.
The Clinical Research Nurse will actively participate in the care of study participants, as well as in the preparation and maintenance of clinical trial documentation, supporting the successful conduct of studies through precise and reliable work.
Responsibilities
Monitor the safety and wellbeing of study participants within the inpatient unit and outpatient/screening facilities
Administer study drugs and concomitant medications in accordance with protocol
Carry out physician orders and respond to medical or psychiatric emergencies where required
Perform and document clinical assessments, including vital signs and electrocardiograms (ECGs)
Maintain accurate and timely documentation of participant status, including progress notes and shift handovers
Ensure continuous accountability of participants while on the unit
Communicate effectively with study staff regarding daily events and participant status
Escalate any abnormal findings to the Investigator or designated staff immediately
Provide study volunteers with clear information on study purpose, procedures, visit schedules, and any dietary or activity restrictions
Support the planning and coordination of in‑clinic stays and outpatient visits
Participate in study team meetings, start‑up activities, and where applicable, audits and inspections
Support the smooth operation of the clinical site, including equipment maintenance, troubleshooting, and arranging replacements where necessary
Sample collection and processing
Collect blood samples via venipuncture and capillary methods
Insert intravenous cannulas where required
Collect pharmacokinetic (PK), pharmacodynamic (PD), and DNA samples in line with protocol and regulatory standards
Process, store, and ship samples in compliance with laboratory manuals and IATA regulations
Operational Support
Maintain organization and oversight of day‑to‑day unit activities
Support scheduling and tracking of in‑house procedures (e.g., urinalysis, drug screening, pregnancy testing)
Assist with study‑related documentation, logs, and sample manifests
Participate in study initiation visits, training sessions, and protocol‑related meetings
Collaborate with the clinical team, Principal Investigator, and Sponsor/CRO to address queries and improve study processes
Support coordination of participant dietary requirements where applicable
Qualifications
Nursing qualification (minimum OKJ 54 or equivalent), valid professional license, and MESZK registration
Minimum of 2 years’ relevant experience, or a combination of education and experience
Clinical research experience strongly preferred
Knowledge of Good Clinical Practice (GCP) requirements
Current training in biohazard waste, bloodborne pathogens, and chemical hygiene preferred
English language skills
Strong verbal and written communication skills
Good interpersonal and problem‑solving abilities
Strong attention to detail and organizational skills, with the ability to work in a fast‑paced environment
Team‑oriented mindset
Office/clinic‑based – Budapest
Benefits
Competitive salary and additional benefits (Cafeteria)
Modern, well‑equipped, and pleasant working conditions
Varied responsibilities with a high level of ownership
Opportunities for professional development
Structured onboarding and training covering clinical research from legal, regulatory, organizational, cultural, and practical perspectives
Additional Benefits Examples
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.
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.
#J-18808-Ljbffr
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.
The Role
As a key member of the clinical unit team, you will support the delivery of clinical trials by ensuring the safety, wellbeing, and accurate monitoring of study participants in both inpatient and outpatient/ambulatory settings, including screening visits. You will work collaboratively with physicians, investigators, and study staff to ensure protocol adherence and high-quality data collection.
The Clinical Research Nurse will actively participate in the care of study participants, as well as in the preparation and maintenance of clinical trial documentation, supporting the successful conduct of studies through precise and reliable work.
Responsibilities
Monitor the safety and wellbeing of study participants within the inpatient unit and outpatient/screening facilities
Administer study drugs and concomitant medications in accordance with protocol
Carry out physician orders and respond to medical or psychiatric emergencies where required
Perform and document clinical assessments, including vital signs and electrocardiograms (ECGs)
Maintain accurate and timely documentation of participant status, including progress notes and shift handovers
Ensure continuous accountability of participants while on the unit
Communicate effectively with study staff regarding daily events and participant status
Escalate any abnormal findings to the Investigator or designated staff immediately
Provide study volunteers with clear information on study purpose, procedures, visit schedules, and any dietary or activity restrictions
Support the planning and coordination of in‑clinic stays and outpatient visits
Participate in study team meetings, start‑up activities, and where applicable, audits and inspections
Support the smooth operation of the clinical site, including equipment maintenance, troubleshooting, and arranging replacements where necessary
Sample collection and processing
Collect blood samples via venipuncture and capillary methods
Insert intravenous cannulas where required
Collect pharmacokinetic (PK), pharmacodynamic (PD), and DNA samples in line with protocol and regulatory standards
Process, store, and ship samples in compliance with laboratory manuals and IATA regulations
Operational Support
Maintain organization and oversight of day‑to‑day unit activities
Support scheduling and tracking of in‑house procedures (e.g., urinalysis, drug screening, pregnancy testing)
Assist with study‑related documentation, logs, and sample manifests
Participate in study initiation visits, training sessions, and protocol‑related meetings
Collaborate with the clinical team, Principal Investigator, and Sponsor/CRO to address queries and improve study processes
Support coordination of participant dietary requirements where applicable
Qualifications
Nursing qualification (minimum OKJ 54 or equivalent), valid professional license, and MESZK registration
Minimum of 2 years’ relevant experience, or a combination of education and experience
Clinical research experience strongly preferred
Knowledge of Good Clinical Practice (GCP) requirements
Current training in biohazard waste, bloodborne pathogens, and chemical hygiene preferred
English language skills
Strong verbal and written communication skills
Good interpersonal and problem‑solving abilities
Strong attention to detail and organizational skills, with the ability to work in a fast‑paced environment
Team‑oriented mindset
Office/clinic‑based – Budapest
Benefits
Competitive salary and additional benefits (Cafeteria)
Modern, well‑equipped, and pleasant working conditions
Varied responsibilities with a high level of ownership
Opportunities for professional development
Structured onboarding and training covering clinical research from legal, regulatory, organizational, cultural, and practical perspectives
Additional Benefits Examples
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.
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.
#J-18808-Ljbffr