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ICON plc

Clinical Research Nurse II

Posted 6 Days Ago
Be an Early Applicant
In-Office or Remote
Hiring Remotely in Washington, USA
Junior
In-Office or Remote
Hiring Remotely in Washington, USA
Junior
Plan, implement, and coordinate clinical research studies. Recruit and assess participants, administer study treatments, collect and record eCRF data, monitor safety, liaise with investigators and regulatory bodies, and provide participant education and support to ensure protocol adherence and regulatory compliance.
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Clinical Research Nurse II

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Clinical Research Nurse II at ICON, you will the planning, implementation, and coordination of clinical research studies, ensuring adherence to protocol requirements and ethical standards, while contributing to the advancement of medical science and patient care.


What You Will Do:

You will contribute to clinical research operations activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Collaborating with study investigators and multidisciplinary teams to develop and execute clinical research protocols, including participant recruitment, enrollment, and follow-up visits
  • Conducting comprehensive patient assessments, administering study treatments and interventions, and monitoring participant safety and well-being throughout the duration of the study
  • Collecting, recording, and analyzing clinical data, including vital signs, laboratory results, and adverse events, in electronic case report forms (eCRFs) and study databases
  • Providing education and support to study participants and their families regarding study procedures, treatment protocols, and informed consent, while addressing any questions or concerns and ensuring adherence to study requirements and timelines.
  • Collaborating with regulatory agencies, ethics committees, and institutional review boards (IRBs) to obtain study approvals, maintain regulatory compliance, and ensure the ethical conduct of clinical research studies

Your Profile:

You will bring relevant clinical research operations experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in Nursing (BSN) from an accredited institution, with current licensure as a Registered Nurse (RN) in the applicable jurisdiction.
  • Minimum of 2-3 years of clinical nursing experience, preferably in a research or academic healthcare setting, with demonstrated knowledge of clinical trial operations, GCP guidelines, and regulatory requirements governing human subjects research.
  • Strong clinical assessment and critical thinking skills, with the ability to independently manage study protocols, prioritize tasks, and make informed decisions in a fast-paced, dynamic environment
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders, including study investigators, research coordinators, and study participants
  • Proficiency in electronic medical record (EMR) systems, data management tools, and Microsoft Office applications, with a high level of attention to detail and accuracy in documenting patient information and study data.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

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Are you a current ICON Employee? Please click here to apply

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