Clinical Research Nurse II/Mid-Wife

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:

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.

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

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