Clinical Research Nurse II

2 weeks ago

San Antonio, Texas, United States ICON Clinical Research Full time
About ICON plc:
ICON plc is a premier organization specializing in healthcare intelligence and clinical research.

We are dedicated to advancing clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and governmental organizations.


With a patient-centric approach, we strive to expedite the development of medications and devices that enhance lives and promote well-being.


Our workforce is our most valuable asset, forming the foundation of our culture and the catalyst for our achievements.

At ICON, our team members are driven by a shared mission and a commitment to excellence in all endeavors.

Our Culture:
We pride ourselves on our diverse teams, which empower us to be better partners to our clients and fulfill our mission of improving patient outcomes.


Our 'Own It' culture is anchored by four core values: Accountability & Delivery, Collaboration, Partnership, and Integrity.

We aspire to be the Clinical Research Organization that consistently delivers exceptional service to our clients and patients alike.

We are in search of talented individuals who resonate with our vision and are eager to contribute to our mission.


The Role:
As a Clinical Research Nurse, you will play a crucial role in the execution of Phase 1 clinical trials. Collaborating closely with research associates, you will gather data from study participants while leveraging your nursing expertise to ensure their safety. Your responsibilities will include administering investigational medications, monitoring vital signs, performing phlebotomy, and conducting examinations as outlined in the study protocol. Additionally, meticulous documentation of collected data and collaboration with study investigators regarding any adverse events will be essential.

Key Responsibilities:
  • Ensure clinical quality, data integrity, and participant safety.
  • Maintain nursing licensure and enhance clinical knowledge and skills.
  • Provide oversight and monitoring of study participants.
  • Administer investigational drugs and other medications in accordance with study protocols.
  • Execute required study procedures effectively.
  • Participate in emergency preparedness drills.
  • Ensure comprehensive documentation to meet all regulatory requirements.
  • Uphold strong ethical standards and safety practices.
  • Engage in peer evaluations, educational programs, and quality improvement initiatives.
  • Review clinical records and conduct quality control assessments.
  • Coordinate and assist in clinical research studies, ensuring adherence to protocols.
  • Communicate with participants to explain study objectives and obtain informed consent.
  • Accurately record clinical data from participants.
  • Collaborate with study investigators on adverse events as per protocol guidelines.
  • Foster communication with internal teams and clinic management.
  • Participate in project meetings with sponsors and project team members.
  • Identify and address equipment and supply deficiencies.
  • Establish and maintain positive relationships with participants and staff.
  • Respond promptly to participant needs.
  • Maintain a clean and organized workspace.
  • Supervise Medical Research Associates and participants during studies, as applicable.
  • Provide shift reports to team members and supervisors.
  • Identify knowledge gaps and performance issues among peers.
  • Mentor and guide clinical staff in study-related tasks and procedures.
  • Assist in managing inventory.
  • Utilize all necessary equipment proficiently for clinical assessments.
  • Perform additional duties as assigned by clinic management.

Qualifications:
  • RN or LPN licensure is required.
  • BLS and ACLS certification at the provider level is required.
  • Strong interpersonal, communication, and problem-solving abilities.
  • Effective written and verbal communication skills.
  • Proficiency in general computer usage is required.

Benefits of Joining ICON:
Our success is rooted in the expertise and quality of our personnel.

We are committed to fostering a culture of continuous learning, where engaging work challenges you and every experience contributes to your professional growth.


At ICON, we offer a comprehensive and competitive total rewards package, which includes not only a competitive base salary but also a variety of variable pay and recognition programs.

Our exceptional employee benefits, supportive policies, and wellness initiatives are designed to support you and your family throughout your career journey.


ICON is an equal opportunity employer, dedicated to creating a workplace free from discrimination and harassment.

All qualified candidates 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 you require reasonable accommodation due to a medical condition or disability during the application process or to perform essential job functions, please inform us through the appropriate channels.

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