What are the responsibilities and job description for the Nurse Midwife position at ICON Strategic Solutions?
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organization, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Nurse Mid-Wife (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.
This role is on-site, part-time in Bothell, WA.
What You Will Do:
- 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:
- Bachelor's degree in Nursing (BSN) from an accredited institution, with current licensure as a Registered Nurse (RN) in the applicable jurisdiction.
- Current Certified Nurse Midwife (CNM) certification is required
- 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 in
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 programs including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
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.
Are you a current ICON Employee? Please click here to apply.