Clinical Research Nurse II

ICON plc • Washington, DC

1d

About The Position

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.

Requirements

• 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.

Responsibilities

• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level