Clinical Research Nurse II/Mid-Wife

Clinical Research Nurse II

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.

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:

The non-expert user will be responsible for:

• Completing and passing both the self-directed and hands-on training before proceeding to scan on study.
  • Must select appropriate sweep protocol based on fundal height.
  • If the uterus is non-palpable (e.g., due to high BMI, thick abdominal wall, or other factors), perform a 5x5 sweep. Document in the free-text section of the paper CRF that the uterus was non-palpable and that a 5x5 sweep was performed for this reason .
• Completing study surveys throughout the study (day of training, 8 weeks post SIV, and end of study).

• Conducting a physical antenatal exam per clinical practice and completing the corresponding CRF.
• Performing a research scan (blind and guided sweeps) SmartSweep per study protocol.

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.

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• 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.

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

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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