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Research Nurse, Senior at Memorial Health Springfield, IL
Job in
Springfield, Sangamon County, Illinois, 62777, USA
Listed on 2026-01-02
Listing for:
Itlearn360
Full Time
position Listed on 2026-01-02
Job specializations:
-
Nursing
Clinical Research Nurse, Nurse Practitioner
Job Description & How to Apply Below
Research Nurse, Senior
Memorial Health, Springfield, IL.
USD $32.95/Hr.
Max USD $52.73/Hr.
Works directly with cancer patients enrolled in clinical trials. Coordinates all aspects of patient care from the start of clinical trial treatment through the duration of the research study. Assists oncology physicians in the clinical management of patient treatment and outcomes. Educates patients about clinical trial options and the risks/benefits of participating in research studies. Performs data management activities for research studies (protocols).
Qualifications- Education:
BSN degree preferred. - Licensure:
Illinois license to practice as Registered Nurse required. - Certification:
Oncology Certified Nurse (OCN) credential or alternate certification in clinical research preferred. - Experience:
Three years recent adult acute care experience required. - Experience:
Two years oncology nursing preferred. - Experience:
Demonstrated clinical experience appropriate to the oncology patient population; must be able to understand and coordinate the multidisciplinary nature of cancer care across settings and disease trajectory. - Experience:
Experience in research data management preferred. - Other Knowledge/Skills/Abilities:
Excellent interpersonal skills, self-initiative, and self-responsibility required. - Other:
Strong organizational and communication skills to manage detailed workflow. - Other:
Ability to think outside the box to arrive at unique solutions to patient care problems and remove barriers to care. - Other:
Must have own transportation for frequent local travel. - Other:
Proven ability to function in autonomous/independent role; highly motivated and self-directed.
- Patient screening and determining eligibility.
- Obtaining informed consent and patient teaching.
- Registering patients on research studies.
- Clinical follow-up and data submission maintenance.
- Quality control regarding documentation, protocol compliance, and data submission requirements.
- Evaluations and analysis of research/data management activities.
Position Requirements
10+ Years
work experience
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